510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K992851Substantially Equivalent

Act Test Catridges for Coaguchek Pro System, Act Controls for Coaguchek Pro System

Roche Diagnostics GmbH, Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992851 is the FDA 510(k) clearance record for ACT TEST CATRIDGES FOR COAGUCHEK PRO SYSTEM, ACT CONTROLS FOR COAGUCHEK PRO SYSTEM, a class II device, cleared for Roche Diagnostics Corp. on under FDA product code JBP (Activated Whole Blood Clotting Time). FDA records list 465 510(k) clearances for Roche Diagnostics Corp., from to . As of , FDA records show no recalls naming K992851.

Clearance record

Decision date
Received
(143 days to decision)
Product code
JBP Activated Whole Blood Clotting Time
Regulation
21 CFR 864.7140
Device class
Class II
Review panel
Hematology
Applicant
Roche Diagnostics Corp. 9115 Hague Rd., P.O. Box 50457, Indianapolis IN
510(k) summary
Summary
Third party review
No

Clearances, product code JBP

Trailing 12 months

FDA records hold no clearances under product code JBP in the trailing twelve months.

FDA records show no clearances under product code JBP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JBP, 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 20260
October 20260