The following data is part of a premarket notification filed by Oem Medical Div. with the FDA for Skin Scrub Kits.
| Device ID | K811855 |
| 510k Number | K811855 |
| Device Name: | SKIN SCRUB KITS |
| Classification | Kit, Surgical Instrument, Disposable |
| Applicant | OEM MEDICAL DIV. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KDD |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-07-01 |
| Decision Date | 1981-07-31 |