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FDA 510(k)

VIS-1000 VIDEO SYSTEM

K-Number: K843806 · 1984-12-12

ApplicantVistek Corp.
Decision Date1984-12-12
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIS-1000 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 1984-12-12 under 510(k) number K843806. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIS-1000 VIDEO SYSTEM?

VIS-1000 VIDEO SYSTEM is a medical device that received FDA 510(k) clearance on 1984-12-12. The listed applicant is Vistek Corp.. The 510(k) number is K843806.

When did VIS-1000 VIDEO SYSTEM receive FDA 510(k) clearance?

VIS-1000 VIDEO SYSTEM received FDA 510(k) clearance on 1984-12-12, under 510(k) number K843806.

Who is the listed applicant for VIS-1000 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-1000 VIDEO SYSTEM?

The FDA product code for VIS-1000 VIDEO SYSTEM is KQM.

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 2000K860173VIS-2000 VIDEO SYSTEM

Related Devices (Code: KQM)

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.

K900160ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTERJedmed Instrument Co.K890826SONY VIDEO GRAPHIC PRINTER UP-850Sony Corp. of AmericaK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDSony Medical Electronics Co.K882958SONY VIDEO PRINTERS, UP SERIESSony Medical Electronics Co.K882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERASM.P. Video, Inc.K873419VIDEO PRINTER SYSTEMTechnology For Imaging, 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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