ARTERIAL BLOOD SAMPLING KIT— 510(k) K832545

Name: FDA 510(k) clearance K832545
Creator: U.S. Food and Drug Administration
Published: 1983-09-26

Substantially Equivalent

Dhd Medical Products Div. Diemolding Corp.

FDA 510(k) clearance K832545 for ARTERIAL BLOOD SAMPLING KIT, Substantially Equivalent on 1983-09-26. Applicant: Dhd Medical Products Div. Diemolding Corp.. Device class: 1.

Clearance details

Applicant: Dhd Medical Products Div. Diemolding Corp.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1983-07-29
Decision date: 1983-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.