The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Ss Agar (modified).
| Device ID | K810931 |
| 510k Number | K810931 |
| Device Name: | SS AGAR (MODIFIED) |
| Classification | Culture Media, Selective And Differential |
| Applicant | OXOID U.S.A., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSI |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-04-06 |
| Decision Date | 1981-04-14 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05032384003433 | K810931 | 000 |