Cleared Traditional

K803059 - INTERSEPT* VENOUS RESERVOIR BAG & HOLDER

K803059 is the FDA 510(k) clearance for INTERSEPT* VENOUS RESERVOIR BAG & HOLDER by Extracorporeal Medical Specialities, Inc.. It is a Class 2 Cardiovascular device (product code DTN) cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K803059 · Extracorporeal Medical Specialities, Inc. · Cardiovascular device
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Dec 1980
Decision
19d
Days
Class 2
Risk

K803059 is an FDA 510(k) clearance for the INTERSEPT* VENOUS RESERVOIR BAG & HOLDER. Classified as Reservoir, Blood, Cardiopulmonary Bypass (product code DTN), Class II - Special Controls.

Submitted by Extracorporeal Medical Specialities, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 22, 1980 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4400 - 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 Extracorporeal Medical Specialities, Inc. devices

Submission Details

510(k) Number K803059 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 03, 1980
Decision Date December 22, 1980
Days to Decision 19 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
106d faster than avg
Panel avg: 125d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DTN Reservoir, Blood, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4400
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 - DTN Reservoir, Blood, Cardiopulmonary Bypass

All 77
Devices cleared under the same product code (DTN) and FDA review panel - the closest regulatory comparables to K803059.
EXV VENOUS RESERVOIR BAG & HOLDER
K823205 · Extracorporeal Medical Specialities, Inc. · Nov 1982
WILLIAM HARVEY FLEX. VENOUS RESERVOIR
K821442 · C.R. Bard, Inc. · Jun 1982
SC-2500F CARDIOTOMY RESERVIOR
K813268 · Scimed Life Systems, Inc. · May 1982
SHILEY UTILITY RESERVOIR
K802119 · Shiley, Inc. · Sep 1980
DISPOSABLE CARDIOTOMY
K781577 · C.R. Bard, Inc. · Sep 1978
CARDIOTOMY RESERVOIR
K780517 · Travenol Laboratories, S.A. · Apr 1978