Cleared Traditional

K780572 - DCG PREAMPLIFIER MODULE

K780572 is the FDA 510(k) clearance for DCG PREAMPLIFIER MODULE by C-V Monitors Corp.. It is a Class 2 Cardiovascular device (product code DRR) cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K780572 · C-V Monitors Corp. · Cardiovascular device
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May 1978
Decision
29d
Days
Class 2
Risk

K780572 is an FDA 510(k) clearance for the DCG PREAMPLIFIER MODULE. Classified as Amplifier And Signal Conditioner, Biopotential (product code DRR), Class II - Special Controls.

Submitted by C-V Monitors Corp. (Mchenry, US). The FDA issued a Cleared decision on May 9, 1978 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2050 - 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 C-V Monitors Corp. devices

Submission Details

510(k) Number K780572 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 10, 1978
Decision Date May 09, 1978
Days to Decision 29 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
96d faster than avg
Panel avg: 125d · This submission: 29d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DRR Amplifier And Signal Conditioner, Biopotential
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2050
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 - DRR Amplifier And Signal Conditioner, Biopotential

All 12
Devices cleared under the same product code (DRR) and FDA review panel - the closest regulatory comparables to K780572.
EPC FILTER
K813123 · Codman & Shurtleff, Inc. · Nov 1981
HP MODEL 8880A FILTER
K802686 · Hewlett-Packard Co. · Nov 1980
MODEL 15055A MAINFRAME
K791964 · Hewlett-Packard Co. · Oct 1979
ESIS MODULE
K780043 · Datascope Corp. · Feb 1978
AMPLIFIER MODULE, 78211A ECG
K772132 · Hewlett-Packard Co. · Nov 1977
ECG AMPLIFIER/R WAVE TRIGGER
K771976 · G.D. Searle and Co. · Nov 1977