The following data is part of a premarket notification filed by American Sterilizer Co. with the FDA for Eagle Steriset.
| Device ID | K823902 |
| 510k Number | K823902 |
| Device Name: | EAGLE STERISET |
| Classification | Wrap, Sterilization |
| Applicant | AMERICAN STERILIZER CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FRG |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-30 |
| Decision Date | 1983-01-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EAGLE STERISET 73595272 1418290 Dead/Cancelled |
AMERICAN STERILIZER COMPANY 1986-04-25 |