STEDIFLO INFUSION SET— 510(k) K832739

Substantially Equivalent

Dravon Medical, Inc.

FDA 510(k) clearance K832739 for STEDIFLO INFUSION SET, Substantially Equivalent on 1983-12-22. Applicant: Dravon Medical, Inc.. Device class: 2.

Clearance details

Applicant: Dravon Medical, Inc.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1983-08-15
Decision date: 1983-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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