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FDA 510(k)

PODIOSCOPE BY ARROW

K-Number: K820119 · 1982-02-18

ApplicantArrow X-Ray Corp.
Decision Date1982-02-18
Product CodeKPW
Advisory CommitteeRA
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 K820119. The device is classified under product code KPW. It was reviewed by the RA advisory panel. 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 K820119.

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 K820119.

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.

What is the FDA product code for PODIOSCOPE BY ARROW?

The FDA product code for PODIOSCOPE BY ARROW is KPW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Arrow X-Ray Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K827069PODIOSCOPE BY ARROW

Related Devices (Code: KPW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K093596LUMOS, MODEL R 72BLumos, Inc.K062788COLLIMATOR, MODEL M-38Umi InternationalK030487R 72Ralco S.R.L.K954310BLA-800AToshiba Medical SystemsK946320R 302Ralco S.R.L.K914184P2020-8-0 BEAM-LIMITING DEVICEPrecise Optics

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.

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