FDA 510(k) Applications Submitted by KEELER INSTRUMENTS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K093298 |
10/21/2009 |
PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000 |
KEELER INSTRUMENTS, INC. |
K100500 |
02/22/2010 |
PSL CLASSIC SLIT LAMP |
KEELER INSTRUMENTS, INC. |
K032087 |
07/07/2003 |
KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004 |
KEELER INSTRUMENTS, INC. |
K970029 |
01/03/1997 |
KEELER SPECTRA INDIRECT OPHTHALMOSCOPE |
KEELER INSTRUMENTS, INC. |
K990257 |
01/27/1999 |
KEELER PULSAIR 3000 NON CONTACT TONOMETER |
KEELER INSTRUMENTS, INC. |
K973064 |
08/18/1997 |
KEELER TEARSCOPE-PLUS |
KEELER INSTRUMENTS, INC. |
K992954 |
09/01/1999 |
KEELER CRYO MASTER & PROBES |
KEELER INSTRUMENTS, INC. |
K060822 |
03/27/2006 |
VANTAGE INDIRECT OPHTHALMOSCOPE |
KEELER INSTRUMENTS, INC. |
K112093 |
07/22/2011 |
CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTER |
KEELER INSTRUMENTS, INC. |
K062412 |
08/17/2006 |
CRYOMATIC |
KEELER INSTRUMENTS, INC. |
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