VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE— 510(k) K873647

Name: FDA 510(k) clearance K873647
Creator: U.S. Food and Drug Administration
Published: 1987-10-20

Substantially Equivalent

Ventrex Laboratories, Inc.

FDA 510(k) clearance K873647 for VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE, Substantially Equivalent on 1987-10-20. Applicant: Ventrex Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code GIO
Device class: Class 1
Regulation: 21 CFR 864.6150
Advisory panel: Hematology
Date received: 1987-09-09
Decision date: 1987-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, ME, US

Download summary PDF View on FDA.gov ↗

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