VENTEX-IA— 510(k) K864641

Substantially Equivalent

Ventech Corp.

FDA 510(k) clearance K864641 for VENTEX-IA, Substantially Equivalent on 1987-01-28. Applicant: Ventech Corp.. Device class: 2.

Clearance details

Applicant: Ventech Corp.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1986-11-26
Decision date: 1987-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Philadelphia, PA, 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.