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 |