GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP— 510(k) K897119

Name: FDA 510(k) clearance K897119
Creator: U.S. Food and Drug Administration
Published: 1990-04-12

Substantially Equivalent

Grieshaber & Co.

FDA 510(k) clearance K897119 for GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP, Substantially Equivalent on 1990-04-12. Applicant: Grieshaber & Co.. Device class: 2.

Clearance details

Applicant: Grieshaber & Co.
Product code: Code HQW
Device class: Class 2
Regulation: 21 CFR 886.3100
Advisory panel: Ophthalmic
Date received: 1989-12-26
Decision date: 1990-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Langhorne, PA, US

Download summary PDF View on FDA.gov ↗

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