KTP/532 LASER FOR OB-GYN USE— 510(k) K874837
Substantially EquivalentLaserscope
FDA 510(k) clearance K874837 for KTP/532 LASER FOR OB-GYN USE, Substantially Equivalent on 1988-03-14. Applicant: Laserscope. Device class: 2.
Clearance details
- Applicant
- Laserscope
- Product code
- Code HHR
- Device class
- Class 2
- Regulation
- 21 CFR 884.4550
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.