UroLift System Procedure Kit Sterilization Tray— 510(k) K192781
Substantially EquivalentNeotract, Inc.
FDA 510(k) clearance K192781 for UroLift System Procedure Kit Sterilization Tray, Substantially Equivalent on 2020-04-14. Applicant: Neotract, Inc.. Device class: 2.
Clearance details
- Applicant
- Neotract, Inc.
- Product code
- Code KCT
- Device class
- Class 2
- Regulation
- 21 CFR 880.6850
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pleasanton, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.