510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850486Substantially Equivalent

General Diag. Chromostrate Heparin Assay

Warner-Lambert Co., Morris Plains NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850486 is the FDA 510(k) clearance record for GENERAL DIAG. CHROMOSTRATE HEPARIN ASSAY, a class II device, cleared for Warner-Lambert Co. on under FDA product code KFF (Assay, Heparin). FDA records list 50 510(k) clearances for Warner-Lambert Co., from to . As of , FDA records show no recalls naming K850486.

Clearance record

Decision date
Received
(90 days to decision)
Product code
KFF Assay, Heparin
Regulation
21 CFR 864.7525
Device class
Class II
Review panel
Hematology
Applicant
Warner-Lambert Co. 201 Tabor Rd., Morris Plains NJ
Third party review
No

Clearances, product code KFF

Trailing 12 months
1 clearance under product code KFF in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KFF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260