510(k) K013976 ยท KDP Regulator, Vacuum
BOEHRINGER MRI SUCTION REGULATORY
| Applicant | Boehringer Laboratories, Norristown PA, US |
| Decision | Substantially Equivalent, Jan 8, 2002 |
| Received | Dec 3, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013976
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.