The following data is part of a premarket notification filed by Kem Medical Products Corp. with the FDA for Biological Indicator - Kemmed & Biosure.
| Device ID | K802228 |
| 510k Number | K802228 |
| Device Name: | BIOLOGICAL INDICATOR - KEMMED & BIOSURE |
| Classification | Indicator, Biological Sterilization Process |
| Applicant | KEM MEDICAL PRODUCTS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRC |
| CFR Regulation Number | 880.2800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-10 |
| Decision Date | 1980-12-09 |