FRINDLEY ENTERPRISE CO— 510(k) K942142

Name: FDA 510(k) clearance K942142
Creator: U.S. Food and Drug Administration
Published: 1995-04-18

Substantially Equivalent

Frindley Enterprise Co., Ltd.

FDA 510(k) clearance K942142 for FRINDLEY ENTERPRISE CO, Substantially Equivalent on 1995-04-18. Applicant: Frindley Enterprise Co., Ltd.. Device class: 1.

Clearance details

Applicant: Frindley Enterprise Co., Ltd.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1994-05-03
Decision date: 1995-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, Taiwan, TW

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