K860349Substantially Equivalent
Lactate Dehydrogenase (Ldh) Reagent Set
Sterling Diagnostics, Inc., Sterling Heights MI / Traditional, Substantially Equivalent
K860349 is the FDA 510(k) clearance record for LACTATE DEHYDROGENASE (LDH) REAGENT SET, a class II device, cleared for Sterling Diagnostics, Inc. on under FDA product code CFH (Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase). FDA records list 41 510(k) clearances for Sterling Diagnostics, Inc., from to . As of , FDA records show no recalls naming K860349.
Clearance record
- Decision date
- Received
- (29 days to decision)
- Product code
- CFH Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase
- Regulation
- 21 CFR 862.1440
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Applicant
- Sterling Diagnostics, Inc. 34210 Dequindre Rd., Sterling Heights MI
- Third party review
- No
Clearances, product code CFH
Trailing 12 monthsFDA records hold no clearances under product code CFH 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.
