UNIVERSAL EYESHIELD— 510(k) K894720

Name: FDA 510(k) clearance K894720
Creator: U.S. Food and Drug Administration
Published: 1989-09-14

Substantially Equivalent

Trident Medical Products, Inc.

FDA 510(k) clearance K894720 for UNIVERSAL EYESHIELD, Substantially Equivalent on 1989-09-14. Applicant: Trident Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Trident Medical Products, Inc.
Product code: Code HOY
Device class: Class 1
Regulation: 21 CFR 886.4750
Advisory panel: Ophthalmic
Date received: 1989-07-25
Decision date: 1989-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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