510(k) K931258 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
SOFTTOUCH II LANCET DEVICE
| Applicant | Boehringer Mannheim Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 10, 1994 |
| Received | Mar 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931258
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.