MERIDIAN-PORTABLE— 510(k) K010897

Substantially Equivalent

Meridian Co., Ltd.

FDA 510(k) clearance K010897 for MERIDIAN-PORTABLE, Substantially Equivalent on 2001-06-19. Applicant: Meridian Co., Ltd..

Clearance details

Applicant: Meridian Co., Ltd.
Product code: Code GZO
Advisory panel: Neurology
Date received: 2001-03-26
Decision date: 2001-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Songpa-Gu, Seoul, KR

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