ANGEION ENDOSCOPIC VALVE SEAL— 510(k) K915719

Substantially Equivalent

Angeion Corp.

FDA 510(k) clearance K915719 for ANGEION ENDOSCOPIC VALVE SEAL, Substantially Equivalent on 1992-02-18. Applicant: Angeion Corp.. Device class: 2.

Clearance details

Applicant: Angeion Corp.
Product code: Code ODC
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1991-12-20
Decision date: 1992-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plymouth, MN, 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.