510(k) K915701 ยท JHI Visual, Pregnancy Hcg, Prescription Use
KODAK SURECELL(TM) HCG URINE TEST KIT/MODIFICATION
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Jan 27, 1992 |
| Received | Dec 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915701
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.