The following data is part of a premarket notification filed by Sterling Diagnostics, Inc. with the FDA for Bun (enzymatic Berthelot) Reagent Set.
| Device ID | K860154 |
| 510k Number | K860154 |
| Device Name: | BUN (ENZYMATIC BERTHELOT) REAGENT SET |
| Classification | Berthelot Indophenol, Urea Nitrogen |
| Applicant | STERLING DIAGNOSTICS, INC. 34210 DEQUINDRE RD. Sterling Heights, MI 48077 |
| Contact | David L Callender |
| Correspondent | David L Callender STERLING DIAGNOSTICS, INC. 34210 DEQUINDRE RD. Sterling Heights, MI 48077 |
| Product Code | CDL |
| CFR Regulation Number | 862.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-16 |
| Decision Date | 1986-02-06 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00811727010568 | K860154 | 000 |