510(k) K800213 ยท KYW Container, Liquid Medication, Graduated
PHARMACY ADDITIVE SYRINGE SET
| Applicant | Cutter Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 26, 1980 |
| Received | Feb 1, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800213
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.