510(k) K855132 ยท MDM Instrument, Manual, Surgical, General Use
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| Applicant | Dynarex Corp., Brewster NY, US |
| Decision | Substantially Equivalent, Jan 24, 1986 |
| Received | Dec 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855132
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.