The following data is part of a premarket notification filed by Pharmacia, Inc. with the FDA for Unicap Phadiatop.
| Device ID | K972364 |
| 510k Number | K972364 |
| Device Name: | UNICAP PHADIATOP |
| Classification | System, Test, Radioallergosorbent (rast) Immunological |
| Applicant | PHARMACIA, INC. 5094 ST. ANDREWS DR. Westervile, OH 43082 |
| Contact | Karen E Martis |
| Correspondent | Karen E Martis PHARMACIA, INC. 5094 ST. ANDREWS DR. Westervile, OH 43082 |
| Product Code | DHB |
| CFR Regulation Number | 866.5750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-25 |
| Decision Date | 1997-09-04 |
| Summary: | summary |