Cleared Traditional

K801944 - MULTICHANNEL TELEMETRY SYSTEM

K801944 is an FDA 510(k) clearance for MULTICHANNEL TELEMETRY SYSTEM, manufactured by Burdick Corp.. The device is a Class 2 Cardiovascular device with product code DRG cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K801944 · Burdick Corp. · Cardiovascular device
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Oct 1980
Decision
70d
Days
Class 2
Risk

K801944 is an FDA 510(k) clearance for the MULTICHANNEL TELEMETRY SYSTEM. Classified as Transmitters And Receivers, Physiological Signal, Radiofrequency (product code DRG), Class II - Special Controls.

Submitted by Burdick Corp. (Mchenry, US). The FDA issued a Cleared decision on October 23, 1980 after a review of 70 days - a notably fast clearance cycle.

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

View all Burdick Corp. devices

FDA 510(k) Submission Details - K801944

510(k) Number K801944 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 14, 1980
Decision Date October 23, 1980
Days to Decision 70 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 125d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRG Device Classification - Class 2, Special Controls

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 Peers - DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

All 71
Devices cleared under the same product code (DRG) and FDA review panel - the closest regulatory comparables to K801944.
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K802273 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1980
KWIK-AWA VEST
K791363 · Medical Specialties, Inc. · Aug 1979
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K790144 · Ge Medical Systems Information Technologies · Feb 1979