Katalyst Cyclophotocoagulation Probe— 510(k) K163632
Substantially EquivalentKatalyst Surgical, LLC
FDA 510(k) clearance K163632 for Katalyst Cyclophotocoagulation Probe, Substantially Equivalent on 2017-06-15. Applicant: Katalyst Surgical, LLC. Device class: 2.
Clearance details
- Applicant
- Katalyst Surgical, LLC
- Product code
- Code LQJ
- Device class
- Class 2
- Regulation
- 21 CFR 886.4390
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chesterfield, MO, US
Recent devices under product code LQJ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.