Cleared Traditional

K050670 - SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS

K050670 is an FDA 510(k) clearance for SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS, manufactured by Tms Telemedizinische Systeme GmbH. The device is a Class 2 Cardiovascular device with product code DXH cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K050670 · Tms Telemedizinische Systeme GmbH · Cardiovascular device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2005
Decision
15d
Days
Class 2
Risk

K050670 is an FDA 510(k) clearance for the SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS. Classified as Transmitters And Receivers, Electrocardiograph, Telephone (product code DXH), Class II - Special Controls.

Submitted by Tms Telemedizinische Systeme GmbH (Chemnitz, DE). The FDA issued a Cleared decision on March 30, 2005 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2920 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K050670

510(k) Number K050670 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 2005
Decision Date March 30, 2005
Days to Decision 15 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 125d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

DXH Device Classification - Class 2, Special Controls

Product Code DXH Transmitters And Receivers, Electrocardiograph, Telephone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2920
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Consultant

Underwriters Laboratories, Inc.
WILLIAM J SAMMONS

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - DXH Transmitters And Receivers, Electrocardiograph, Telephone

All 284
Devices cleared under the same product code (DXH) and FDA review panel - the closest regulatory comparables to K050670.
CARDIONAVIGATOR +
K051960 · Del Mar Reynolds Medical, Ltd. · Aug 2005
MEDSTAR 220, MODEL 533-220
K050951 · Cibernet Systems Corp. · Jul 2005
PMP4 MEDICAL WEB CENTER
K050940 · Card Guard Scientific Survival , Ltd. · Jul 2005
PMP4 SELFCHECK ECG
K042254 · Card Guard Scientific Survival , Ltd. · Jan 2005
VST3
K040942 · Biowatch Medical, Inc. · Sep 2004
E-TAC EX-1000 ELECTROCARDIOGRAPHIC EVENT RECORDER
K042022 · Datrix, Inc. Dba of Jon Barron, Inc. · Aug 2004
K050670 · SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS
Download PDF FDA Summary Tms Telemedizinische …