Keeler Instruments, Inc. - FDA 510(k) Cleared Devices
60
Total
60
Cleared
0
Denied
Keeler Instruments, Inc. has 60 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.
Historical record: 60 cleared submissions from 1981 to 2019.
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) cleared devices by Keeler Instruments, Inc.
60 devices
Cleared
Feb 08, 2019
Keeler TonoCare Tonometer
Ophthalmic
283d
Cleared
Dec 08, 2011
CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTER
Ophthalmic
139d
Cleared
Dec 10, 2010
PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000
Ophthalmic
415d
Cleared
Mar 09, 2010
PSL CLASSIC SLIT LAMP
Ophthalmic
15d
Cleared
Nov 06, 2006
CRYOMATIC
Ophthalmic
81d
Cleared
May 23, 2006
VANTAGE INDIRECT OPHTHALMOSCOPE
Ophthalmic
57d
Cleared
Nov 26, 2003
KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004
Ophthalmic
142d
Cleared
Dec 21, 1999
KEELER CRYO MASTER & PROBES
Ophthalmic
111d
Cleared
Mar 25, 1999
KEELER PULSAIR 3000 NON CONTACT TONOMETER
Ophthalmic
57d
Cleared
Apr 07, 1998
KEELER TEARSCOPE-PLUS
Ophthalmic
232d
Cleared
Apr 02, 1997
KEELER SPECTRA INDIRECT OPHTHALMOSCOPE
Ophthalmic
89d
Cleared
Nov 22, 1994
KEELER MULTILASE 3000
Ophthalmic
202d
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