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FDA 510(k) Applications Submitted by HOWARD INSTRUMENTS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030948
03/26/2003
VMATE MODEL VMM1000
HOWARD INSTRUMENTS, INC.
K063104
08/10/2006
FOX MEDICAL DIODE LASER SYSTEM 810NM
HOWARD INSTRUMENTS, INC.
K974598
12/09/1997
MICROKERATOME OR THE MATE
HOWARD INSTRUMENTS, INC.
K980985
03/17/1998
SCMD-1000
HOWARD INSTRUMENTS, INC.
K972727
07/21/1997
CBALK-1000 BLADE
HOWARD INSTRUMENTS, INC.
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