510(k) K936138 ยท JHI Visual, Pregnancy Hcg, Prescription Use
KODAK SURECELL HCG-SERUM/URINE TEST KIT, MODIFICATION
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Apr 8, 1994 |
| Received | Dec 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936138
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.