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FDA 510(k)

AD/V IMAGEPLEX(TM)

K-Number: K943158 · 1994-11-22

ApplicantAdaptive Video, Inc.
Decision Date1994-11-22
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AD/V IMAGEPLEX(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Adaptive Video, Inc.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K943158. 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 AD/V IMAGEPLEX(TM)?

AD/V IMAGEPLEX(TM) is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Adaptive Video, Inc.. The 510(k) number is K943158.

When did AD/V IMAGEPLEX(TM) receive FDA 510(k) clearance?

AD/V IMAGEPLEX(TM) received FDA 510(k) clearance on 1994-11-22, under 510(k) number K943158.

Who is the listed applicant for AD/V IMAGEPLEX(TM)?

The FDA 510(k) record lists Adaptive Video, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AD/V IMAGEPLEX(TM)?

The FDA product code for AD/V IMAGEPLEX(TM) 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 Adaptive Video, Inc. 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.

K925799AD/V A.5K921877AD/V SPOOLER

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

View on FDA Database →

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

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