GY-RO SAFE— 510(k) K883785

Substantially Equivalent

Gy-Ro Industry, Inc.

FDA 510(k) clearance K883785 for GY-RO SAFE, Substantially Equivalent on 1989-01-05. Applicant: Gy-Ro Industry, Inc.. Device class: 1.

Clearance details

Applicant: Gy-Ro Industry, Inc.
Product code: Code HOG
Device class: Class 1
Regulation: 21 CFR 886.4070
Advisory panel: Ophthalmic
Date received: 1988-09-07
Decision date: 1989-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOG

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K834354 — OPHTEC RUST RING REMOVER1984-03-19

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