MICROSURGICAL CYSTOTOME— 510(k) K890218

Name: FDA 510(k) clearance K890218
Creator: U.S. Food and Drug Administration
Published: 1989-01-27

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890218 for MICROSURGICAL CYSTOTOME, Substantially Equivalent on 1989-01-27. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1989-01-18
Decision date: 1989-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

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K890387 — MALLEABLE PLACENTA CURETTE1989-02-27

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