510(k) K082056 ยท FFX System, Gastrointestinal Motility (Electrical)
ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
| Applicant | Life-Tech, Inc., Stafford TX, US |
| Decision | Substantially Equivalent, Nov 7, 2008 |
| Received | Jul 21, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082056
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.