SATURN ACTIVE LASER SYSTEM— 510(k) K083208

Substantially Equivalent

Research Instruments , Ltd.

FDA 510(k) clearance K083208 for SATURN ACTIVE LASER SYSTEM, Substantially Equivalent on 2009-08-25. Applicant: Research Instruments , Ltd..

Clearance details

Applicant: Research Instruments , Ltd.
Product code: Code MRX
Advisory panel: Obstetrics/Gynecology
Date received: 2008-10-31
Decision date: 2009-08-25
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Falmouth, Cornwall, GB

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