510(k) DEN980003 ยท MVH Device, Detection, Sulfide
DIAMOND PROBE/PERIO 2000 SYSTEM
| Applicant | Diamond General Development Corp., Ann Arbor MI, US |
| Decision | Unknown, Jul 17, 1998 |
| Received | May 18, 1998 |
| Type | Post-NSE |
| FDA record | Open on fda.gov |
Recalls that name DEN980003
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.