SOLO BAND LIGATOR— 510(k) K960020

Substantially Equivalent

Surcraft, LLC

FDA 510(k) clearance K960020 for SOLO BAND LIGATOR, Substantially Equivalent on 1996-04-01. Applicant: Surcraft, LLC. Device class: 2.

Clearance details

Applicant: Surcraft, LLC
Product code: Code FHN
Device class: Class 2
Regulation: 21 CFR 876.4400
Advisory panel: Gastroenterology, Urology
Date received: 1996-01-02
Decision date: 1996-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport News, VA, 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.