KIT,I.V. START— 510(k) K940035

Unknown

Mason-Keller Corp.

FDA 510(k) clearance K940035 for KIT,I.V. START, Unknown on 1994-06-03. Applicant: Mason-Keller Corp.. Device class: 1.

Clearance details

Applicant: Mason-Keller Corp.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1994-01-04
Decision date: 1994-06-03
Decision: Unknown
Clearance type: Traditional
Location: Roseland, NJ, 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.