510(k) K162721 ยท NRB Wound Cleaner, Ultrasound
Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator
| Applicant | Alliqua Biomedical, Inc., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Dec 22, 2016 |
| Received | Sep 29, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162721
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.