510(k) K082366 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
LIFEBED PATIENT VIGILANCE SYSTEM
| Applicant | Hoana Medical, Inc., Honolulu HI, US |
| Decision | Substantially Equivalent, Sep 26, 2008 |
| Received | Aug 18, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082366
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.