The following data is part of a premarket notification filed by Fraser Sweatman, Inc. with the FDA for Absorber, Anesthesia Circle Sys, Co2.
| Device ID | K760076 |
| 510k Number | K760076 |
| Device Name: | ABSORBER, ANESTHESIA CIRCLE SYS, CO2 |
| Classification | Absorber, Carbon-dioxide |
| Applicant | FRASER SWEATMAN, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BSF |
| CFR Regulation Number | 868.5310 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-18 |
| Decision Date | 1976-07-16 |