SUCTION-HEMORRHOID-LIGATOR— 510(k) K832192

Name: FDA 510(k) clearance K832192
Creator: U.S. Food and Drug Administration
Published: 1983-12-27

Substantially Equivalent

Research Endoscope Systems Intl.

FDA 510(k) clearance K832192 for SUCTION-HEMORRHOID-LIGATOR, Substantially Equivalent on 1983-12-27. Applicant: Research Endoscope Systems Intl.. Device class: 2.

Clearance details

Applicant: Research Endoscope Systems Intl.
Product code: Code FHN
Device class: Class 2
Regulation: 21 CFR 876.4400
Advisory panel: Gastroenterology, Urology
Date received: 1983-07-08
Decision date: 1983-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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