The following data is part of a premarket notification filed by Sterling Diagnostics, Inc. with the FDA for Lactate Dehydrogenase (ldh) Reagent Set (uv Rate).
Device ID | K862255 |
510k Number | K862255 |
Device Name: | LACTATE DEHYDROGENASE (LDH) REAGENT SET (UV RATE) |
Classification | Nad Reduction/nadh Oxidation, Lactate Dehydrogenase |
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 | CFJ |
CFR Regulation Number | 862.1440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-06-13 |
Decision Date | 1986-07-29 |