Cleared Traditional

K781764 - PAD, COOLING #27-999

K781764 is an FDA 510(k) clearance for PAD, manufactured by Cobe Laboratories, Inc.. The device is a Class 2 Cardiovascular device with product code DTR cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K781764 · Cobe Laboratories, Inc. · Cardiovascular device
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Dec 1978
Decision
49d
Days
Class 2
Risk

K781764 is an FDA 510(k) clearance for the PAD, COOLING #27-999. Classified as Heat-exchanger, Cardiopulmonary Bypass (product code DTR), Class II - Special Controls.

Submitted by Cobe Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 4, 1978 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4240 - 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 Cobe Laboratories, Inc. devices

FDA 510(k) Submission Details - K781764

510(k) Number K781764 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 16, 1978
Decision Date December 04, 1978
Days to Decision 49 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
76d faster than avg
Panel avg: 125d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTR Device Classification - Class 2, Special Controls

Product Code DTR Heat-exchanger, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4240
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 - DTR Heat-exchanger, Cardiopulmonary Bypass

All 83
Devices cleared under the same product code (DTR) and FDA review panel - the closest regulatory comparables to K781764.
CARDIOPLEGIA DELIVERY SYSTEM
K800377 · 3M Health Care, Sarns · Mar 1980
MINIPRIME HYPOTHERMIC HEAT EXCHANGER
K791430 · Travenol Laboratories, S.A. · Aug 1979
HEAT EXCHANGER COIL
K790756 · Delta Medical Industries · Jun 1979
HEAT EXCHANGER, FHX-14
K781210 · Delta Medical Industries · Oct 1978
HEAT EXCHANGER, DISP., OMNITHERM
K772117 · Scimed Life Systems, Inc. · Mar 1978
PACING KIT, ELECATH TRANSTHORACIC
K770016 · Electro-Catheter Corp. · Jan 1977