PODIOSCOPE BY ARROW— 510(k) K820119

Substantially Equivalent

Arrow X-Ray Corp.

FDA 510(k) clearance K820119 for PODIOSCOPE BY ARROW, Substantially Equivalent on 1982-02-18. Applicant: Arrow X-Ray Corp.. Device class: 2.

Clearance details

Applicant: Arrow X-Ray Corp.
Product code: Code KPW
Device class: Class 2
Regulation: 21 CFR 892.1610
Advisory panel: Radiology
Date received: 1982-01-18
Decision date: 1982-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Arrow X-Ray Corp.

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