The following data is part of a premarket notification filed by Microbio-medics, Inc. with the FDA for Microtek Probe Drape.
| Device ID | K882724 |
| 510k Number | K882724 |
| Device Name: | MICROTEK PROBE DRAPE |
| Classification | Drape, Surgical |
| 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 | KKX |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-01 |
| Decision Date | 1988-08-03 |