FDA 510(k)

PODIOSCOPE BY ARROW

K-Number: K827069 · 1982-02-18

Decision Date1982-02-18

Product Code

DecisionSubstantially Equivalent

Device Summary

PODIOSCOPE BY ARROW is the device name listed in this FDA 510(k) record. The listed applicant is Arrow X-Ray Corp.. It received FDA 510(k) clearance on 1982-02-18 under 510(k) number K827069. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PODIOSCOPE BY ARROW?

PODIOSCOPE BY ARROW is a medical device that received FDA 510(k) clearance on 1982-02-18. The listed applicant is Arrow X-Ray Corp.. The 510(k) number is K827069.

When did PODIOSCOPE BY ARROW receive FDA 510(k) clearance?

PODIOSCOPE BY ARROW received FDA 510(k) clearance on 1982-02-18, under 510(k) number K827069.

Who is the listed applicant for PODIOSCOPE BY ARROW?

The FDA 510(k) record lists Arrow X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Arrow X-Ray Corp. as applicant

K820119PODIOSCOPE BY ARROW

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.