Cleared Traditional

VitalConnect Platform, VitalPatch Biosensor (K183078) - FDA 510(k) Clearance

Class II Cardiovascular device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K183078 · Vitalconnect, Inc. · Cardiovascular device
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Mar 2019
Decision
122d
Days
Class 2
Risk

K183078 is an FDA 510(k) clearance for the VitalConnect Platform, VitalPatch Biosensor. Classified as Transmitters And Receivers, Physiological Signal, Radiofrequency (product code DRG), Class II - Special Controls.

Submitted by Vitalconnect, Inc. (San Jose, US). The FDA issued a Cleared decision on March 7, 2019 after a review of 122 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2910 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Vitalconnect, Inc. devices

Submission Details

510(k) Number K183078 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 2018
Decision Date March 07, 2019
Days to Decision 122 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
3d faster than avg
Panel avg: 125d · This submission: 122d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DRG Transmitters And Receivers, Physiological Signal, Radiofrequency
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2910
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

Medical Device Academy, Inc.
Robert Packard

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 - DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

All 57
Devices cleared under the same product code (DRG) and FDA review panel - the closest regulatory comparables to K183078.
BioSticker System
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Life Sensor Cardiac Monitor
K191331 · Braveheart Wireless, Inc. · Jun 2019
VitalPatch 7D Biosensor - single, VitalPatch 7D Biosensor - bag of 20
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Surveyor S2
K182297 · Mortara Instrument, Inc. · Jan 2019
Comarch e-Care Platform
K181248 · Comarch Healthcare SA · Oct 2018
Caretaker Remote Display App and Caretaker Software Library
K181196 · Caretaker Medical, LLC · Oct 2018