Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K951293Substantially Equivalent

Quantitate Enzyme Verifier Set

Beckman Instruments, Inc., Brea CA / Traditional, Substantially Equivalent

K951293 is the FDA 510(k) clearance record for QUANTITATE ENZYME VERIFIER SET, a class I device, cleared for Beckman Instruments, Inc. on under FDA product code JJT (Enzyme Controls (Assayed And Unassayed)). FDA records list 281 510(k) clearances for Beckman Instruments, Inc., from to . As of , FDA records show no recalls naming K951293.

Clearance record

Decision date
Received
(29 days to decision)
Product code
JJT Enzyme Controls (Assayed And Unassayed)
Regulation
21 CFR 862.1660
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Beckman Instruments, Inc. 200 S. Kraemer Blvd., W-337, Brea CA
510(k) summary
Summary
Third party review
No

Clearances, product code JJT

Trailing 12 months

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

FDA records show no clearances under product code JJT in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JJT, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260