The following data is part of a premarket notification filed by Pharmacia, Inc. with the FDA for Phadebact Csf Test.
| Device ID | K844999 |
| 510k Number | K844999 |
| Device Name: | PHADEBACT CSF TEST |
| Classification | Antisera, All Groups, N. Meningitidis |
| Applicant | PHARMACIA, INC. 800 CENTENNIAL AVE. Piscataway, NJ 08854 -3911 |
| Contact | Albert P Mayo |
| Correspondent | Albert P Mayo PHARMACIA, INC. 800 CENTENNIAL AVE. Piscataway, NJ 08854 -3911 |
| Product Code | GTJ |
| CFR Regulation Number | 866.3390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-12-26 |
| Decision Date | 1985-10-17 |