The following data is part of a premarket notification filed by Microtek Medical, Inc. with the FDA for Antrum & Attic Mirror.
| Device ID | K833601 |
| 510k Number | K833601 |
| Device Name: | ANTRUM & ATTIC MIRROR |
| Classification | Mirror, Ent |
| Applicant | MICROTEK MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KAI |
| CFR Regulation Number | 874.4420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-12 |
| Decision Date | 1984-01-03 |