The following data is part of a premarket notification filed by Derma Media Lab., Inc. with the FDA for Lactate Dehydrogenase.
Device ID | K964912 |
510k Number | K964912 |
Device Name: | LACTATE DEHYDROGENASE |
Classification | Nad Reduction/nadh Oxidation, Lactate Dehydrogenase |
Applicant | DERMA MEDIA LAB., INC. 8531 WELLSFORD PL., SUITE E Santa Fe Springs, CA 90670 |
Contact | Charles C Allain, Ph.d. |
Correspondent | Charles C Allain, Ph.d. DERMA MEDIA LAB., INC. 8531 WELLSFORD PL., SUITE E Santa Fe Springs, CA 90670 |
Product Code | CFJ |
CFR Regulation Number | 862.1440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-12-09 |
Decision Date | 1997-01-09 |