MICROSURGICAL KERATOME— 510(k) K890216

Name: FDA 510(k) clearance K890216
Creator: U.S. Food and Drug Administration
Published: 1989-02-16

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890216 for MICROSURGICAL KERATOME, Substantially Equivalent on 1989-02-16. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code GZX
Device class: Class 1
Regulation: 21 CFR 882.4525
Advisory panel: Neurology
Date received: 1989-01-18
Decision date: 1989-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

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K890382 — COMPRESSION FORCEPS1989-02-27
K890387 — MALLEABLE PLACENTA CURETTE1989-02-27

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