ANESTY 10— 510(k) K880744

Substantially Equivalent

Nihon Medix Co., Ltd.

FDA 510(k) clearance K880744 for ANESTY 10, Substantially Equivalent on 1989-02-09. Applicant: Nihon Medix Co., Ltd.. Device class: 2.

Clearance details

Applicant: Nihon Medix Co., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-02-24
Decision date: 1989-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hopewell Junction, NY, US

Download summary PDF View on FDA.gov ↗

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