510(k) K083351 ยท DQA Oximeter
PROABLE PULSE OXIMETER, MODEL MD-600P, TRAVELER OXIMETER, MODEL MD-650P AND PALM PULSE OXIMETER, MODEL MD-680P
| Applicant | Comdek Industrial Corp., Taipei, TW |
| Decision | Substantially Equivalent, Apr 24, 2009 |
| Received | Nov 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083351
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.