OREXAS POTENTEST— 510(k) K830158

Name: FDA 510(k) clearance K830158
Creator: U.S. Food and Drug Administration
Published: 1983-02-07

Substantially Equivalent

Orexas Medical Corp.

FDA 510(k) clearance K830158 for OREXAS POTENTEST, Substantially Equivalent on 1983-02-07. Applicant: Orexas Medical Corp.. Device class: Unclassified.

Clearance details

Applicant: Orexas Medical Corp.
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1983-01-18
Decision date: 1983-02-07
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.