510(k) K880253 ยท FEF Tube, Single Lumen, With Mercury Wt Balloon For Intestinal Intubation And / Or Decompression
BLAKEMORE RETAINER
| Applicant | Orthopedic Systems, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Mar 11, 1988 |
| Received | Jan 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880253
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.