The following data is part of a premarket notification filed by Sa Scientific, Inc. with the FDA for Sas Salmonella 0 Factor 8 Antiserum And/or Sas Salmonella 0 Group C2 Factor 9 Antiserum.
| Device ID | K960138 |
| 510k Number | K960138 |
| Device Name: | SAS SALMONELLA 0 FACTOR 8 ANTISERUM AND/OR SAS SALMONELLA 0 GROUP C2 FACTOR 9 ANTISERUM |
| Classification | Antisera, All Groups, Salmonella Spp. |
| Applicant | SA SCIENTIFIC, INC. 4919 GOLDEN QUAIL San Antonio, TX 78240 |
| Contact | Harbi Shadfan |
| Correspondent | Harbi Shadfan SA SCIENTIFIC, INC. 4919 GOLDEN QUAIL San Antonio, TX 78240 |
| Product Code | GRM |
| CFR Regulation Number | 866.3550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-11 |
| Decision Date | 1996-03-06 |