The following data is part of a premarket notification filed by Bio-analytics Laboratories, Inc. with the FDA for Ldh-l Liquid Enzymatic, Kinetic Kit.
Device ID | K810083 |
510k Number | K810083 |
Device Name: | LDH-L LIQUID ENZYMATIC, KINETIC KIT |
Classification | Nad Reduction/nadh Oxidation, Lactate Dehydrogenase |
Applicant | BIO-ANALYTICS LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CFJ |
CFR Regulation Number | 862.1440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-01-13 |
Decision Date | 1981-01-28 |