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FDA 510(k)

IDXVIEW

K-Number: K954071 · 1996-02-27

ApplicantIdx Systems Corp.
Decision Date1996-02-27
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IDXVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Idx Systems Corp.. It received FDA 510(k) clearance on 1996-02-27 under 510(k) number K954071. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDXVIEW?

IDXVIEW is a medical device that received FDA 510(k) clearance on 1996-02-27. The listed applicant is Idx Systems Corp.. The 510(k) number is K954071.

When did IDXVIEW receive FDA 510(k) clearance?

IDXVIEW received FDA 510(k) clearance on 1996-02-27, under 510(k) number K954071.

Who is the listed applicant for IDXVIEW?

The FDA 510(k) record lists Idx Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IDXVIEW?

The FDA product code for IDXVIEW is LMD.

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 Idx Systems 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.

K052618IMAGECAST PACS

Related Devices (Code: LMD)

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.

K994329IIVS INTEGRATED IMAGE VIEWING STATIONTerarecon,Inc.K992698STENTOR, PAGEVIEWStentor, Inc.K992426RAYPAX WEB CLINICAL SYSTEMSamsung Sds Co., Ltd.K992352ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0Inteleradiology, Inc.K991537SAMSUNG RAYPAX SYSTEMSamsung Sds Co., Ltd.K984000STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEMSurgical Navigation Technologies, Inc.

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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