The following data is part of a premarket notification filed by Sterling Diagnostics, Inc. with the FDA for Amylase Reagent Set (modified Caraway).
| Device ID | K860530 |
| 510k Number | K860530 |
| Device Name: | AMYLASE REAGENT SET (MODIFIED CARAWAY) |
| Classification | Amyloclastic, Amylase |
| 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 | CJA |
| CFR Regulation Number | 862.1070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-02-12 |
| Decision Date | 1986-02-28 |