510(k) K882539 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
CLEANTECH SYSTEM
| Applicant | Schiff & Co., West Cadwell NJ, US |
| Decision | Substantially Equivalent, Aug 8, 1988 |
| Received | Jun 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882539
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.