Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K896921Substantially Equivalent

Raichem Tm Hemoglobin Calibrator

Reagents Applications, Inc., San Diego CA / Traditional, Substantially Equivalent

K896921 is the FDA 510(k) clearance record for RAICHEM TM HEMOGLOBIN CALIBRATOR, a class II device, cleared for Reagents Applications, Inc. on under FDA product code KRZ (Calibrator For Hemoglobin And Hematocrit Measurement). FDA records list 63 510(k) clearances for Reagents Applications, Inc., from to . As of , FDA records show no recalls naming K896921.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KRZ Calibrator For Hemoglobin And Hematocrit Measurement
Regulation
21 CFR 864.8165
Device class
Class II
Review panel
Hematology
Applicant
Reagents Applications, Inc. 8225 Mercury Ct., San Diego CA
Third party review
No

Clearances, product code KRZ

Trailing 12 months

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

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