510(k) K950754 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
MACRO SUCTION TUBE MODEL NO 10061
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Apr 25, 1995 |
| Received | Feb 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950754
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.