Trek Medical Products, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Trek Medical Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Milwaukee, US.
Historical record: 8 cleared submissions from 1986 to 1992.
Browse the FDA 510(k) cleared devices submitted by Trek Medical Products, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Oct 02, 1992
COMPUTERIZED PUPIL
Ophthalmic
218d
Cleared
May 29, 1992
FTS-200 GAS SYSTEM
Anesthesiology
88d
Cleared
Sep 19, 1990
RAPID AUTOMATIC PNEUMOPERITONEUM-I
Obstetrics & Gynecology
210d
Cleared
Sep 12, 1990
FIBER OPTIC LIGHT SOURCE
Ear, Nose, Throat
78d
Cleared
Apr 30, 1990
GLAUCOMA MECHANICAL TREPHINE
Ophthalmic
210d
Cleared
Sep 09, 1988
OPHTHALMIC FLUID INJECTOR
General Hospital
91d
Cleared
Mar 07, 1988
OPHTHALMIC LIGHT PIPE PICK
General & Plastic Surgery
81d
Cleared
Dec 15, 1986
VES-10 INTRAOCULAR SCISSORS DRIVE
Ophthalmic
60d