TUTTIFRUTTI (NON-PRES. SUNGLASSES)— 510(k) K801922

Name: FDA 510(k) clearance K801922
Creator: U.S. Food and Drug Administration
Published: 1980-11-12

Substantially Equivalent

Safety Plastics of New York

FDA 510(k) clearance K801922 for TUTTIFRUTTI (NON-PRES. SUNGLASSES), Substantially Equivalent on 1980-11-12. Applicant: Safety Plastics of New York. Device class: 1.

Clearance details

Applicant: Safety Plastics of New York
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1980-08-12
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code HQY

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K974852 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974860 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974861 — NON-PRESCRIPTION SUNGLASSES1998-01-27
K974511 — SUNGLASSES1998-01-12
K974441 — SUNGLASSES1998-01-09

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