The following data is part of a premarket notification filed by Stanbio Laboratory with the FDA for Alkaline Phosphatase Test Set.
| Device ID | K772257 |
| 510k Number | K772257 |
| Device Name: | ALKALINE PHOSPHATASE TEST SET |
| Classification | Thymolphthalein Monophosphate, Alkaline Phosphatase Or Isoenzymes |
| Applicant | STANBIO LABORATORY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CIO |
| CFR Regulation Number | 862.1050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-05 |
| Decision Date | 1977-12-22 |