PAIN VISION, MODEL PS-2100— 510(k) K072882

Substantially Equivalent

Osachi Co., Ltd.

FDA 510(k) clearance K072882 for PAIN VISION, MODEL PS-2100, Substantially Equivalent on 2009-01-08. Applicant: Osachi Co., Ltd.. Device class: 1.

Clearance details

Applicant: Osachi Co., Ltd.
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 2007-10-09
Decision date: 2009-01-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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