510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K964457Substantially Equivalent

Roche Cobas Ibtegra Reagent Cassettes

Roche Diagnostic Systems, Inc., Branchburg NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K964457 is the FDA 510(k) clearance record for ROCHE COBAS IBTEGRA REAGENT CASSETTES, a class I device, cleared for Roche Diagnostic Systems, Inc. on under FDA product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase). FDA records list 296 510(k) clearances for Roche Diagnostic Systems, Inc., from to . As of , FDA records show 2 recalls naming K964457.

Clearance record

Decision date
Received
(68 days to decision)
Product code
JQB Kinetic Method, Gamma-Glutamyl Transpeptidase
Regulation
21 CFR 862.1360
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Roche Diagnostic Systems, Inc. 1080 Us Hwy. 202, Branchburg NJ
510(k) summary
Summary
Third party review
No

Clearances, product code JQB

Trailing 12 months

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

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