Cleared Traditional

K780116 - AMPLIFIER

K780116 is an FDA 510(k) clearance for AMPLIFIER, manufactured by Burdick Corp.. The device is a Class 1 Cardiovascular device with product code DQC cleared through the Traditional 510(k) pathway after a 35-day FDA review.

K780116 · Burdick Corp. · Cardiovascular device
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Feb 1978
Decision
35d
Days
Class 1
Risk

K780116 is an FDA 510(k) clearance for the AMPLIFIER, PC-700. Classified as Phonocardiograph (product code DQC), Class I - General Controls.

Submitted by Burdick Corp. (Mchenry, US). The FDA issued a Cleared decision on February 24, 1978 after a review of 35 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2390 - 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 - K780116

510(k) Number K780116 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 1978
Decision Date February 24, 1978
Days to Decision 35 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
90d faster than avg
Panel avg: 125d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

DQC Device Classification - Class 1, General Controls

Product Code DQC Phonocardiograph
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 870.2390
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - DQC Phonocardiograph

Devices cleared under the same product code (DQC) and FDA review panel - the closest regulatory comparables to K780116.
ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE
K900560 · Acuson Corp. · Dec 1990
MEDDARS/ULTRA IMAGER PULSE/PHON MODULE
K811626 · Honeywell, Inc. · Jul 1981
NIC-200 VENTRICULAR FUNCTION ANALYZER
K792466 · Nicolet Biomedical Instruments · Jan 1980
PULSE/PHONOCARDIOGRAPHY CHANNEL, 144
K770757 · Honeywell, Inc. · May 1977
PHON/STRESS SYSTEM (#21126A)
K760464 · Hewlett-Packard Co. · Aug 1976