The following data is part of a premarket notification filed by I.a.f. Production, Inc. with the FDA for Iafp Mueller Hinton Agar W/hemo. W/cva Enrichment.
| Device ID | K872687 |
| 510k Number | K872687 |
| Device Name: | IAFP MUELLER HINTON AGAR W/HEMO. W/CVA ENRICHMENT |
| Classification | Culture Media, Antimicrobial Susceptibility Test |
| Applicant | I.A.F. PRODUCTION, INC. 527, BOUL. DES PRAIRIES Laval, Que. H7n-423, CA |
| Contact | Francois Morin |
| Correspondent | Francois Morin I.A.F. PRODUCTION, INC. 527, BOUL. DES PRAIRIES Laval, Que. H7n-423, CA |
| Product Code | LKA |
| CFR Regulation Number | 866.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-07-07 |
| Decision Date | 1987-08-11 |