510(k) K971111 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER
| Applicant | Tri-Tech, Inc., Southport NC, US |
| Decision | Substantially Equivalent, Jun 16, 1997 |
| Received | Mar 26, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971111
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.