Kowa Optimed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kowa Optimed, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Kowa Optimed, Inc. has 10 FDA 510(k) cleared ophthalmic devices. Based in Torrance, US.
Historical record: 10 cleared submissions from 1988 to 2002.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kowa Optimed, Inc.
10 devices
Cleared
Oct 11, 2002
KOWA AUTOMATED TONOMETER KT-500
Ophthalmic
330d
Cleared
Jun 17, 1996
AUTOMATIC VISUAL FIELD PLOTTER AP-125
Ophthalmic
90d
Cleared
Jun 04, 1996
KOWA HAND-HELD APPLANATION TONOMETER HA-1
Ophthalmic
90d
Cleared
Jan 03, 1996
KOWA SC-1200 PHOTO SLIT LAMP SYSTEM
Ophthalmic
36d
Cleared
Dec 01, 1995
KOWA PROFESSIONAL FUNDUS CAMERA MODELS FX-500, FX-500S, FX-500C
Ophthalmic
45d
Cleared
Dec 01, 1995
KOWA GENESIS HAND-HELD FUNDUS CAMERA
Ophthalmic
45d
Cleared
Nov 24, 1995
KOWA PORTABLE SLIT LAMP SL-14 & SL-14B
Ophthalmic
38d
Cleared
Feb 07, 1992
LASER FLARE METER
Ophthalmic
164d
Cleared
Sep 27, 1988
LASER FLARE CELL METER FC-1000
Ophthalmic
207d
Cleared
May 03, 1988
AUTOMATIC PERIMETER, AP-340
Ophthalmic
42d