The following data is part of a premarket notification filed by Katalyst Surgical, Llc with the FDA for Katalyst Laser Probes, Katalyst Illuminated Laser Probes.
| Device ID | K121187 |
| 510k Number | K121187 |
| Device Name: | KATALYST LASER PROBES, KATALYST ILLUMINATED LASER PROBES |
| Classification | Laser, Ophthalmic |
| Applicant | KATALYST SURGICAL, LLC 1331 H ST NW, 12TH FL Washington, DC 20005 |
| Contact | Michelle Mcdonough |
| Correspondent | Michelle Mcdonough KATALYST SURGICAL, LLC 1331 H ST NW, 12TH FL Washington, DC 20005 |
| Product Code | HQF |
| Subsequent Product Code | HQB |
| Subsequent Product Code | MPA |
| CFR Regulation Number | 886.4390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-04-19 |
| Decision Date | 2012-09-17 |
| Summary: | summary |