VENTRE/SEP— 510(k) K811423

Substantially Equivalent

Ventrex Laboratories, Inc.

FDA 510(k) clearance K811423 for VENTRE/SEP, Substantially Equivalent on 1981-06-09. Applicant: Ventrex Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code CFP
Device class: Class 1
Regulation: 21 CFR 862.1405
Advisory panel: Clinical Chemistry
Date received: 1981-05-21
Decision date: 1981-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Ventrex Laboratories, Inc.

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