510(k) K933507 ยท EJK Liner, Cavity, Calcium Hydroxide
NEEDLETUBE SYRINGE CARTRTIDGE
| Applicant | Centrix, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jan 18, 1994 |
| Received | Jul 15, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933507
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.