510(k) K880704 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
CERULLO SUCTION REGULATOR
| Applicant | Aesculap Instruments Corp., Burlingame CA, US |
| Decision | Substantially Equivalent, Mar 29, 1988 |
| Received | Feb 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880704
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.