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FDA 510(k)

VISTEK ELECTRONIC CONTROLLER

K-Number: K904682 · 1990-12-18

ApplicantVistek Corp.
Decision Date1990-12-18
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VISTEK ELECTRONIC CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Vistek Corp.. It received FDA 510(k) clearance on 1990-12-18 under 510(k) number K904682. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTEK ELECTRONIC CONTROLLER?

VISTEK ELECTRONIC CONTROLLER is a medical device that received FDA 510(k) clearance on 1990-12-18. The listed applicant is Vistek Corp.. The 510(k) number is K904682.

When did VISTEK ELECTRONIC CONTROLLER receive FDA 510(k) clearance?

VISTEK ELECTRONIC CONTROLLER received FDA 510(k) clearance on 1990-12-18, under 510(k) number K904682.

Who is the listed applicant for VISTEK ELECTRONIC CONTROLLER?

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 VISTEK ELECTRONIC CONTROLLER?

The FDA product code for VISTEK ELECTRONIC CONTROLLER is GEY.

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 SOURCEK871034LCA 2000K860173VIS-2000 VIDEO SYSTEMK843806VIS-1000 VIDEO SYSTEM

Related Devices (Code: GEY)

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.

K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDSArthrocare Corp.K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)DepuyacromedK972308MEDNEXT 1000 DRILLMednext, Inc.K971941AQUA SPRAYBoyd Industries, Inc.K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., 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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