VENTREX ALLERGEN DISC— 510(k) K924119

Substantially Equivalent

Ventrex, Inc.

FDA 510(k) clearance K924119 for VENTREX ALLERGEN DISC, Substantially Equivalent on 1992-11-30. Applicant: Ventrex, Inc.. Device class: 2.

Clearance details

Applicant: Ventrex, Inc.
Product code: Code DHB
Device class: Class 2
Regulation: 21 CFR 866.5750
Advisory panel: Immunology
Date received: 1992-08-14
Decision date: 1992-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, ME, 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.