510(k) K123308 ยท JOW Sleeve, Limb, Compressible
PULSTAR LOGIX INTERMITTENT PNEUMATIC COMPRESSION SYSTEM
| Applicant | Albahealth, LLC, Rockwood TN, US |
| Decision | Substantially Equivalent, Feb 8, 2013 |
| Received | Oct 24, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123308
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.