NOSITE UV INTERIM SPECTACLES— 510(k) K823825

Name: FDA 510(k) clearance K823825
Creator: U.S. Food and Drug Administration
Published: 1983-02-24

Substantially Equivalent

Patton, Boggs & Blow

FDA 510(k) clearance K823825 for NOSITE UV INTERIM SPECTACLES, Substantially Equivalent on 1983-02-24. Applicant: Patton, Boggs & Blow. Device class: 1.

Clearance details

Applicant: Patton, Boggs & Blow
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1982-12-20
Decision date: 1983-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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