MODEL S139029 SUNGLASSES W/MIRROR ACRYLIC LENSES— 510(k) K900527

Name: FDA 510(k) clearance K900527
Creator: U.S. Food and Drug Administration
Published: 1990-05-03

Substantially Equivalent

J & B Assoc.

FDA 510(k) clearance K900527 for MODEL S139029 SUNGLASSES W/MIRROR ACRYLIC LENSES, Substantially Equivalent on 1990-05-03. Applicant: J & B Assoc.. Device class: 1.

Clearance details

Applicant: J & B Assoc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1990-02-02
Decision date: 1990-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQY

view all

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

More clearances from J & B Assoc.

view all

K900520 — MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS1990-05-03
K900521 — MODEL N742 SUNGLASSES W/POLYCARBONATE BLUE BLOCKER1990-05-03
K900522 — MODEL N741 SUNGLASSES W/ACRYLIC BLUE COMPUTER LENS1990-05-03
K900524 — MODEL F3 FLIP UP SUNGLASSES W/POLORIZED COMPUTER1990-05-03
K900526 — MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS1990-05-03

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