510(k) K953929 ยท LIO Device, Specimen Collection
MID-STREAM COLLECTION SET-STERILE
| Applicant | Trinity Laboratories, Inc., Salisbury MD, US |
| Decision | Substantially Equivalent, Nov 16, 1995 |
| Received | Aug 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953929
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.