FITO DIDO— 510(k) K963075

Substantially Equivalent

Framesmart, Inc.

FDA 510(k) clearance K963075 for FITO DIDO, Substantially Equivalent on 1996-08-22. Applicant: Framesmart, Inc.. Device class: 1.

Clearance details

Applicant: Framesmart, Inc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1996-07-24
Decision date: 1996-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, 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

More clearances from Framesmart, Inc.

K962912 — MARCELLA CARAN1996-08-22

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