Cleared Traditional

K884766 - BERICHROM PLASMINOGEN

K884766 is the FDA 510(k) clearance for BERICHROM PLASMINOGEN by Behring Diagnostics, Inc.. It is a Class 1 Immunology device (product code DDX) cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K884766 · Behring Diagnostics, Inc. · Immunology device
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Jan 1989
Decision
51d
Days
Class 1
Risk

K884766 is an FDA 510(k) clearance for the BERICHROM(R) PLASMINOGEN. Classified as Plasminogen, Antigen, Antiserum, Control (product code DDX), Class I - General Controls.

Submitted by Behring Diagnostics, Inc. (Somerville, US). The FDA issued a Cleared decision on January 4, 1989 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5715 - the FDA immunology device 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 Behring Diagnostics, Inc. devices

Submission Details

510(k) Number K884766 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1988
Decision Date January 04, 1989
Days to Decision 51 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 104d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DDX Plasminogen, Antigen, Antiserum, Control
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.5715
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 - DDX Plasminogen, Antigen, Antiserum, Control

All 7
Devices cleared under the same product code (DDX) and FDA review panel - the closest regulatory comparables to K884766.
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K850410 · Warner-Lambert Co. · May 1985
ACA PLASMINOGEN TEST PACK
K812625 · E.I. Dupont DE Nemours & Co., Inc. · Sep 1981
HELENA PLASMINOGEN QUIPLATE PROCEDURE
K811777 · Helena Laboratories · Jul 1981
PLASMINOGEN ASSAY
K781478 · Dade, Baxter Travenol Diagnostics, Inc. · Nov 1978