510(k) K073664 ยท MDM Instrument, Manual, Surgical, General Use
FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCER
| Applicant | Injectimed, Inc., Albuquerque NM, US |
| Decision | Substantially Equivalent, Aug 8, 2008 |
| Received | Dec 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073664
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.