The following data is part of a premarket notification filed by Bio-analytics Laboratories, Inc. with the FDA for Alkaline Phosph., Liquid Enzy., Kin. Kit.
| Device ID | K810082 |
| 510k Number | K810082 |
| Device Name: | ALKALINE PHOSPH., LIQUID ENZY., KIN. KIT |
| Classification | Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes |
| Applicant | BIO-ANALYTICS LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CJE |
| CFR Regulation Number | 862.1050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-01-13 |
| Decision Date | 1981-01-26 |