K972639Substantially Equivalent
Tina-Quant Haptoglobin
Boehringer Mannheim Corp., Concord CA / Traditional, Substantially Equivalent
K972639 is the FDA 510(k) clearance record for TINA-QUANT HAPTOGLOBIN, a class II device, cleared for Boehringer Mannheim Corp. on under FDA product code DAD (Haptoglobin, Antigen, Antiserum, Control). FDA records list 340 510(k) clearances for Boehringer Mannheim Corp., from to . As of , FDA records show no recalls naming K972639.
Clearance record
- Decision date
- Received
- (178 days to decision)
- Product code
- DAD Haptoglobin, Antigen, Antiserum, Control
- Regulation
- 21 CFR 866.5460
- Device class
- Class II
- Review panel
- Immunology
- Applicant
- Boehringer Mannheim Corp. 2380a Bisso Ln., Concord CA
- 510(k) summary
- Summary
- Third party review
- No
Clearances, product code DAD
Trailing 12 monthsFDA records hold no clearances under product code DAD 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.
