The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Mcbride Medium Cm 819.
| Device ID | K872135 |
| 510k Number | K872135 |
| Device Name: | MCBRIDE MEDIUM CM 819 |
| Classification | Culture Media, Selective And Non-differential |
| Applicant | OXOID U.S.A., INC. 9017 RED BRANCH RD. Columbia, MD 21045 |
| Contact | Ruth Kemp |
| Correspondent | Ruth Kemp OXOID U.S.A., INC. 9017 RED BRANCH RD. Columbia, MD 21045 |
| Product Code | JSJ |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-06-03 |
| Decision Date | 1987-06-15 |