510(k) K171334 ยท PHL Powered Exoskeleton
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| Applicant | Parker Hannifin Corporation, Macedonia OH, US |
| Decision | Substantially Equivalent, Sep 8, 2017 |
| Received | May 8, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171334
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.