UMBILICAL CORD BLOOD SAMPLING KIT— 510(k) K900302

Name: FDA 510(k) clearance K900302
Creator: U.S. Food and Drug Administration
Published: 1990-04-10

Substantially Equivalent

Ge Medical Systems Information Technologies

FDA 510(k) clearance K900302 for UMBILICAL CORD BLOOD SAMPLING KIT, Substantially Equivalent on 1990-04-10. Applicant: Ge Medical Systems Information Technologies. Device class: 1.

Clearance details

Applicant: Ge Medical Systems Information Technologies
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1990-01-22
Decision date: 1990-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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