510(k) K002890 ยท GEX Powered Laser Surgical Instrument
INTRALASE 600C LASER KERATOME
| Applicant | Intra Lase Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 9, 2001 |
| Received | Sep 15, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002890
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 12, 2003 | Intralase Corp Intralase FS Laser System.
Laser Keratome Terminated |
GEX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.