510(k) K082789 ยท DQA Oximeter
G1B PULSE OXIMETER
| Applicant | General Meditech, Inc., Shanghai, CN |
| Decision | Substantially Equivalent, Jan 7, 2009 |
| Received | Sep 23, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082789
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.