510(k) K834522 ยท ESE Larynx, Artificial (Battery-Powered)
VENTI-VOICE NASAL CATHETER
| Applicant | Respiratory Support Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 17, 1984 |
| Received | Dec 21, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834522
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.