The following data is part of a premarket notification filed by Sterling Diagnostics, Inc. with the FDA for Alt (sgpt) Reagent Set (uv Rate).
Device ID | K862209 |
510k Number | K862209 |
Device Name: | ALT (SGPT) REAGENT SET (UV RATE) |
Classification | Nadh Oxidation/nad Reduction, Alt/sgpt |
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 | CKA |
CFR Regulation Number | 862.1030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-06-10 |
Decision Date | 1986-06-25 |