Howard Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Howard Instruments, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Howard Instruments, Inc. has 5 FDA 510(k) cleared medical devices. Based in Tuscaloosa, US.
Historical record: 5 cleared submissions from 1997 to 2007. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Howard Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Howard Instruments, Inc.
5 devices
Cleared
May 16, 2007
FOX MEDICAL DIODE LASER SYSTEM 810NM
General & Plastic Surgery
279d
Cleared
Jun 17, 2003
VMATE MODEL VMM1000
Ophthalmic
83d
Cleared
May 01, 1998
SCMD-1000
Ophthalmic
45d
Cleared
Apr 22, 1998
MICROKERATOME OR THE MATE
Ophthalmic
134d
Cleared
Oct 10, 1997
CBALK-1000 BLADE
Ophthalmic
81d