SATURN ACTIVE LASER SYSTEM— 510(k) K083208
Substantially EquivalentResearch Instruments , Ltd.
FDA 510(k) clearance K083208 for SATURN ACTIVE LASER SYSTEM, Substantially Equivalent on 2009-08-25. 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
- Abbreviated
- Location
- Falmouth, Cornwall, GB
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More clearances from Research Instruments , Ltd.
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