The following data is part of a premarket notification filed by Gibson Laboratories, Inc. with the FDA for P And T Medium.
| Device ID | K904773 |
| 510k Number | K904773 |
| Device Name: | P AND T MEDIUM |
| Classification | System, Transport, Aerobic |
| Applicant | GIBSON LABORATORIES, INC. 1040 MANCHESTER ST. Lexington, KY 40508 |
| Contact | Cecil Gibson |
| Correspondent | Cecil Gibson GIBSON LABORATORIES, INC. 1040 MANCHESTER ST. Lexington, KY 40508 |
| Product Code | JTW |
| CFR Regulation Number | 866.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-22 |
| Decision Date | 1990-12-04 |