SATURN 3 LASER SYSTEM— 510(k) K060764
Substantially EquivalentResearch Instruments , Ltd.
FDA 510(k) clearance K060764 for SATURN 3 LASER SYSTEM, Substantially Equivalent on 2007-03-12. Applicant: Research Instruments , Ltd.. Device class: 2.
Clearance details
- Applicant
- Research Instruments , Ltd.
- Product code
- Code MRX
- Device class
- Class 2
- Regulation
- 21 CFR 884.6200
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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More clearances from Research Instruments , Ltd.
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