510(k) K122060 ยท CAF Nebulizer (Direct Patient Interface)
CLEVER TD-7001NEBULIZER
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Mar 21, 2013 |
| Received | Jul 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122060
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.