510(k) K892504 ยท LRC Instrument, Ent Manual Surgical
'EXMOOR' SINGLE USE SUCTION TUBE
| Applicant | Exmoor Plastics , Ltd., Taunton, GB |
| Decision | Substantially Equivalent, Jun 22, 1989 |
| Received | Apr 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892504
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.