Medical Device Manufacturer · US , Cambridge , MA

Tomey Corporation USA - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1991

Total

Cleared

Denied

Tomey Corporation USA has 9 FDA 510(k) cleared medical devices. Based in Cambridge, US.

Historical record: 9 cleared submissions from 1991 to 1997. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Tomey Corporation USA Filter by specialty or product code using the sidebar.

Tomey Corporation USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tomey Corporation USA

9 devices

1-9 of 9

IMAGESCAPE DIGITAL RETINAL IMAGE SYSTEM

TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4

K932571 · GWE

Neurology · 826d

Cleared Mar 01, 1995

VIDEO VISION ANALYZER (VIVA), VRB 100

K945959 · HKO

Ophthalmic · 84d

Cleared Nov 22, 1994

TOMEY EM-1000 SPECULAR MICROSCOPE

K944910 · HJO

Ophthalmic · 48d

Cleared Apr 05, 1993

TOMEY PROTON TONOMETER

K924760 · HKY

Ophthalmic · 194d

Cleared Jul 15, 1992

TOMEY PE-300 PORTABLE ERG

K921815 · HLT

Ophthalmic · 91d

Cleared Jun 17, 1991

PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480

K912112 · LQJ

Ophthalmic · 35d

Tomey Corporation USA - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Tomey Corporation USA

Filters