The following data is part of a premarket notification filed by Anaerobe Systems with the FDA for Mueller Hinton Agar W/wo Blood.
| Device ID | K841137 |
| 510k Number | K841137 |
| Device Name: | MUELLER HINTON AGAR W/WO BLOOD |
| Classification | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/broth |
| Applicant | ANAEROBE SYSTEMS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JTZ |
| CFR Regulation Number | 866.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-03-16 |
| Decision Date | 1984-03-26 |