Cleared Traditional

K931254 - GOGGLE SAFEGUARD
(FDA 510(k) Clearance)

Nov 1993
Decision
245d
Days
Class 1
Risk

K931254 is an FDA 510(k) clearance for the GOGGLE SAFEGUARD. This device is classified as a Shield, Eye, Ophthalmic (including Sunlamp Protective Eyewear And Post-mydriatic Eyewear) (Class I - General Controls, product code HOY).

Submitted by Sellstrom Mfg. Co. (Palatine, US). The FDA issued a Cleared decision on November 12, 1993, 245 days after receiving the submission on March 12, 1993.

This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.4750.

Submission Details

510(k) Number K931254 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 1993
Decision Date November 12, 1993
Days to Decision 245 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement

Device Classification

Product Code HOY — Shield, Eye, Ophthalmic (including Sunlamp Protective Eyewear And Post-mydriatic Eyewear)
Device Class Class I - General Controls
CFR Regulation 21 CFR 886.4750

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