Cleared Traditional

MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER (K873423) - FDA 510(k) Clearance

Class II Cardiovascular device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K873423 · Johnson & Johnson Professionals, Inc. · Cardiovascular device
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Nov 1987
Decision
73d
Days
Class 2
Risk

K873423 is an FDA 510(k) clearance for the MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER. Classified as Reservoir, Blood, Cardiopulmonary Bypass (product code DTN), Class II - Special Controls.

Submitted by Johnson & Johnson Professionals, Inc. (King Of Prussia, US). The FDA issued a Cleared decision on November 6, 1987 after a review of 73 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 Johnson & Johnson Professionals, Inc. devices

Submission Details

510(k) Number K873423 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 25, 1987
Decision Date November 06, 1987
Days to Decision 73 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
52d faster than avg
Panel avg: 125d · This submission: 73d
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 50
Devices cleared under the same product code (DTN) and FDA review panel - the closest regulatory comparables to K873423.
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K893711 · Shiley, Inc. · Feb 1990
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K896414 · Baxter Healthcare Corp · Jan 1990
DIDECO-SHILEY AUTOTRANSFUSION CARDIOTOMY RESERVOIR
K884872 · Shiley, Inc. · Jan 1989
EXPANDED USE OF HARDSHELL VENOUS RESERV. W/FILTER
K872719 · Shiley, Inc. · Sep 1987
SHILEY PTS CHEST DRAINAGE AUTOTRANSFUSION SET
K872720 · Shiley, Inc. · Sep 1987
EXPANDED USE FOR SHILEY 3L CARDIOTOMY RESERVOIR
K872721 · Shiley, Inc. · Sep 1987