MENICON PROGENT REMOVER— 510(k) K002140

Substantially Equivalent

Menicon Co, Ltd.

FDA 510(k) clearance K002140 for MENICON PROGENT REMOVER, Substantially Equivalent on 2000-10-10. Applicant: Menicon Co, Ltd..

Clearance details

Applicant: Menicon Co, Ltd.
Product code: Code MRC
Advisory panel: Ophthalmic
Date received: 2000-07-17
Decision date: 2000-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, MA, US

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