Vistech Consultants, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Vistech Consultants, Inc. makes
Vistech Consultants, Inc. produces visual contrast sensitivity and glare testing devices, including the VCTS 700S System, VCTS 6000, and MCT 8000 Multi-Vision Contrast Tester. These devices are designed to assess potential acuity and glare sensitivity in clinical settings.
The company's products are regulated as Class I devices and are listed in the FDA 510(k) registry. Vistech Consultants, Inc. is based in the United States.
Catalogue
Visual Contrast Sensiti., Potential Acuity&Glare Ref K882634
Regimes: 510(k) Registry: 510(k)Vistech Vcts Glare Tester Ref K853481
Regimes: 510(k) Registry: 510(k)Vcts Marketing Program System Ref K881022
Regimes: 510(k) Registry: 510(k)Vcts 700S System Ref K881021
Regimes: 510(k) Registry: 510(k)Vistech Vcts 6000 Ref K840255
Regimes: 510(k) Registry: 510(k)Mct 8000 (Multi-Vision Contrast Tester) Ref K881059
Regimes: 510(k) Registry: 510(k)Vcts 6500 System Ref K881023
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vistech Consultants, Inc. have in the registry?
The registry currently lists 7 devices for Vistech Consultants, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vistech Consultants, Inc.'s devices?
Among its 7 most recently registered devices, Vistech Consultants, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Vistech Consultants, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Vistech Consultants, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vistech Consultants, Inc. in the registry?
The most recently registered devices listed for Vistech Consultants, Inc. include VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE, VISTECH VCTS GLARE TESTER, VCTS MARKETING PROGRAM SYSTEM and VCTS 700S SYSTEM.