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FDA 510(k)

VIS-2000 VIDEO SYSTEM

K-Number: K860173 · 1986-02-07

ApplicantVistek Corp.
Decision Date1986-02-07
Product CodeFWG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIS-2000 VIDEO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vistek Corp.. It received FDA 510(k) clearance on 1986-02-07 under 510(k) number K860173. The device is classified under product code FWG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIS-2000 VIDEO SYSTEM?

VIS-2000 VIDEO SYSTEM is a medical device that received FDA 510(k) clearance on 1986-02-07. The listed applicant is Vistek Corp.. The 510(k) number is K860173.

When did VIS-2000 VIDEO SYSTEM receive FDA 510(k) clearance?

VIS-2000 VIDEO SYSTEM received FDA 510(k) clearance on 1986-02-07, under 510(k) number K860173.

Who is the listed applicant for VIS-2000 VIDEO SYSTEM?

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

What is the FDA product code for VIS-2000 VIDEO SYSTEM?

The FDA product code for VIS-2000 VIDEO SYSTEM is FWG.

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 Vistek 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.

K904681VLS 5300 300W XENON LIGHT SOURCEK904682VISTEK ELECTRONIC CONTROLLERK871034LCA 2000K843806VIS-1000 VIDEO SYSTEM

Related Devices (Code: FWG)

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.

K9348833D VIDEO SYSTEMRichard Wolf Medical Instruments Corp.

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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