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  |