510(k) K031023 ยท HQF Laser, Ophthalmic
PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10
| Applicant | Peregrine Surgical , Ltd., New Britain PA, US |
| Decision | Substantially Equivalent, Jun 27, 2003 |
| Received | Mar 31, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031023
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 14, 2021 | Dutch Ophthalmic USA, Inc. Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system
Product Code: 7510.ALC Open, Classified |
HQF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.