510(k) K021323 ยท DQX Wire, Guide, Catheter
MODIFICATION TO SAFE-STEER GUIDE WIRE SYSTEM
| Applicant | Intra Luminal Therapeutics, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, May 22, 2002 |
| Received | Apr 26, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021323
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.