Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VISTECH VCTS 6000

K-Number: K840255 · 1984-04-13

ApplicantVistech Consultants, Inc.
Decision Date1984-04-13
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISTECH VCTS 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Vistech Consultants, Inc.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840255. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTECH VCTS 6000?

VISTECH VCTS 6000 is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Vistech Consultants, Inc.. The 510(k) number is K840255.

When did VISTECH VCTS 6000 receive FDA 510(k) clearance?

VISTECH VCTS 6000 received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840255.

Who is the listed applicant for VISTECH VCTS 6000?

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

What is the FDA product code for VISTECH VCTS 6000?

The FDA product code for VISTECH VCTS 6000 is HOX.

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 Vistech Consultants, 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.

K882634VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLAREK881059MCT 8000 (MULTI-VISION CONTRAST TESTER)K881021VCTS 700S SYSTEMK881022VCTS MARKETING PROGRAM SYSTEMK881023VCTS 6500 SYSTEMK853481VISTECH VCTS GLARE TESTER

View all 7 devices →

Related Devices (Code: HOX)

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.

K100095CENTRAL VISION ANALYZER MODEL 1000Vimetrics,Llc.K944156HEINE LAMBDA 100Heine USA , Ltd.K881971OCCU-TECH VISION TESTApplied Vision Concepts, Inc.K883337PL 20/20 INFANT VISION TESTEROptimed Technologies, Inc.K882634VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLAREVistech Consultants, Inc.K881358PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAMNeuroscientific Corp.

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.

↑