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 monthsFDA records hold no clearances under product code KRZ in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
