The following data is part of a premarket notification filed by Microbio-medics, Inc. with the FDA for Microtek Reuter-style Bi-valve Intranasal Splint.
| Device ID | K895502 |
| 510k Number | K895502 |
| Device Name: | MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT |
| Classification | Splint, Nasal |
| Applicant | MICROBIO-MEDICS, INC. POST OFFICE BOX 2487 Columbus, MS 39704 |
| Contact | Keith Mcgee |
| Correspondent | Keith Mcgee MICROBIO-MEDICS, INC. POST OFFICE BOX 2487 Columbus, MS 39704 |
| Product Code | EPP |
| CFR Regulation Number | 874.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-12 |
| Decision Date | 1989-12-08 |