510(k) K123738 ยท CAW Generator, Oxygen, Portable
MARK 5 NUVO LITE OCSI, MARK 5 NUVO LITE STD
| Applicant | Nidek Medical Products, Inc., Birmingham AL, US |
| Decision | Substantially Equivalent, Feb 28, 2013 |
| Received | Dec 5, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123738
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.