The following data is part of a premarket notification filed by American Monitor Corp. with the FDA for Kinetic Alkaline Phosphatase.
| Device ID | K834033 |
| 510k Number | K834033 |
| Device Name: | KINETIC ALKALINE PHOSPHATASE |
| Classification | Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes |
| Applicant | AMERICAN MONITOR CORP. 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 | 1983-11-23 |
| Decision Date | 1984-01-30 |