The following data is part of a premarket notification filed by Clinical Data, Inc. with the FDA for In Vitro Tests For Phosphatase & Blood Nitrogen.
| Device ID | K852441 |
| 510k Number | K852441 |
| Device Name: | IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN |
| Classification | Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes |
| Applicant | CLINICAL DATA, INC. 1172 COMMONWEALTH AVE. Boston, MA 02134 |
| Contact | Israel M Stein |
| Correspondent | Israel M Stein CLINICAL DATA, INC. 1172 COMMONWEALTH AVE. Boston, MA 02134 |
| Product Code | CJE |
| CFR Regulation Number | 862.1050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-06-10 |
| Decision Date | 1985-08-21 |