Vistech Consultants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vistech Consultants, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Vistech Consultants, Inc. has 7 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 7 cleared submissions from 1984 to 1988. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vistech Consultants, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vistech Consultants, Inc.
7 devices
Cleared
Jul 15, 1988
VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE
Ophthalmic
18d
Cleared
Apr 04, 1988
MCT 8000 (MULTI-VISION CONTRAST TESTER)
Ophthalmic
24d
Cleared
Apr 01, 1988
VCTS 700S SYSTEM
Ophthalmic
22d
Cleared
Apr 01, 1988
VCTS MARKETING PROGRAM SYSTEM
Ophthalmic
22d
Cleared
Apr 01, 1988
VCTS 6500 SYSTEM
Ophthalmic
22d
Cleared
Oct 29, 1985
VISTECH VCTS GLARE TESTER
Ophthalmic
70d
Cleared
Apr 13, 1984
VISTECH VCTS 6000
Ophthalmic
81d