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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