VENTURE II MONITORING SYSTEM— 510(k) K830321

Substantially Equivalent

Rae Medical Corp.

FDA 510(k) clearance K830321 for VENTURE II MONITORING SYSTEM, Substantially Equivalent on 1983-06-03. Applicant: Rae Medical Corp.. Device class: 1.

Clearance details

Applicant: Rae Medical Corp.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1983-01-31
Decision date: 1983-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.