510(k) K091880 ยท MQC Mouthguard, Prescription
CLAYTON INTRA-AURAL DEVICE (CID)
| Applicant | Ascentia Health Incorporated, Springfield VA, US |
| Decision | Substantially Equivalent, Feb 24, 2010 |
| Received | Jun 24, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091880
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.