THE GRIESHABER AXIAL CUTTER— 510(k) K950056

Substantially Equivalent

Grieshaber & Co.

FDA 510(k) clearance K950056 for THE GRIESHABER AXIAL CUTTER, Substantially Equivalent on 1995-05-05. Applicant: Grieshaber & Co.. Device class: 2.

Clearance details

Applicant: Grieshaber & Co.
Product code: Code HKP
Device class: Class 2
Regulation: 21 CFR 886.4150
Advisory panel: Ophthalmic
Date received: 1995-01-06
Decision date: 1995-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kennesaw, GA, US

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