NON-PRESCRIPTION SUNGLASSES— 510(k) K942588

Substantially Equivalent

Pro Axess

FDA 510(k) clearance K942588 for NON-PRESCRIPTION SUNGLASSES, Substantially Equivalent on 1994-07-12. Applicant: Pro Axess. Device class: 1.

Clearance details

Applicant: Pro Axess
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1994-06-01
Decision date: 1994-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Valley City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQY

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.