Instrumed, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Instrumed, Inc. has 7 FDA 510(k) cleared medical devices. Based in Union Bridge, US.
Historical record: 7 cleared submissions from 1986 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Instrumed, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jul 11, 1995
CLEAN-CUFF
General & Plastic Surgery
71d
Cleared
May 19, 1995
ACCUTEST
General & Plastic Surgery
459d
Cleared
Jan 12, 1993
ACCUFLATE
General & Plastic Surgery
141d
Cleared
Nov 25, 1992
ACCUFLATE ACCESSORIE CART W/IV POLE AND CLAMP
Anesthesiology
89d
Cleared
Feb 19, 1991
ACCUFLATE
General & Plastic Surgery
14d
Cleared
Jan 24, 1989
DISPOSABLE COLOR-CUFFS
General & Plastic Surgery
21d
Cleared
Mar 03, 1986
POLYPET
Microbiology
12d