510(k) K770369 ยท CBD Bottle, Collection, Breathing System (Calibrated)
VACON TM
| Applicant | Diemolding Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 1, 1977 |
| Received | Feb 24, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770369
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.