510(k) K880754 ยท EHZ Evacuator, Oral Cavity
DRI-CLAVE LIQUID KLEENZALL
| Applicant | Columbus Dental Mfg. Co., St. Louis MO, US |
| Decision | Substantially Equivalent, May 12, 1988 |
| Received | Feb 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880754
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.