SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P.— 510(k) K875063

Name: FDA 510(k) clearance K875063
Creator: U.S. Food and Drug Administration
Published: 1988-02-22

Substantially Equivalent

Epson EL Paso, Inc.

FDA 510(k) clearance K875063 for SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P., Substantially Equivalent on 1988-02-22. Applicant: Epson EL Paso, Inc.. Device class: 1.

Clearance details

Applicant: Epson EL Paso, Inc.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1987-12-09
Decision date: 1988-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: El Paso, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.