Neitz Instruments Company, Ltd. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neitz Instruments Company, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CATARACTSCREENER CT - S, NEITZ SLIT LAMP SL-H2, FIBER HEAD LIGHT FH-300
24
Total
24
Cleared
0
Denied
Neitz Instruments Company, Ltd. has 24 FDA 510(k) cleared ophthalmic devices. Based in Washington, US.
Historical record: 24 cleared submissions from 1994 to 1997.
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 - Neitz Instruments Company, Ltd.
24 devices
Cleared
Sep 30, 1997
CATARACTSCREENER CT - S
Ophthalmic
92d
Cleared
Jun 15, 1995
NEITZ SLIT LAMP SL-H2
Ophthalmic
83d
Cleared
Jun 08, 1995
FIBER HEAD LIGHT FH-300
Ophthalmic
76d
Cleared
May 03, 1995
OTOSCOPE A-34
Ear, Nose, Throat
71d
Cleared
Apr 10, 1995
NEITZ SLIT LAMP SL-H1
Ophthalmic
17d
Cleared
Apr 07, 1995
INDIRECT OPHTHALMOSCOPE VIDEO SYSTEM IO0 A TV
Ophthalmic
14d
Cleared
Mar 28, 1995
STREAK RETINOSCOPE RX-1
Ophthalmic
35d
Cleared
Mar 28, 1995
STREAK RETINOSCOPE RX-3
Ophthalmic
35d
Cleared
Mar 28, 1995
STREAK RETINOSCOPE RX-3A
Ophthalmic
35d
Cleared
Mar 28, 1995
SPOT RETINOSCOPE RX-3SP
Ophthalmic
35d
Cleared
Mar 28, 1995
STREAK RETINOSCOPE RX-RC
Ophthalmic
35d
Cleared
Mar 28, 1995
STREAK RETINOSCOPE RX-RP
Ophthalmic
35d