Teknomed, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Teknomed, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1979 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Teknomed, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
May 21, 1993
TECHNOMED PULSOLITH 4000 LASER SYSTEM
General Hospital
207d
Cleared
Nov 05, 1992
MULTILASE 2100 C, 2100 D
General & Plastic Surgery
429d
Cleared
Nov 05, 1992
MULTILASE 2500 A
General & Plastic Surgery
261d
Cleared
Feb 21, 1992
MULTILASE 2100 A
General & Plastic Surgery
212d
Cleared
Oct 06, 1989
TECHNOMED PULSOLITH LASER SYSTEM
Gastroenterology & Urology
57d
Cleared
Mar 23, 1989
TECHNOMED PULSOLITH LASER SYSTEM
Gastroenterology & Urology
55d
Cleared
Feb 21, 1979
TECNOTOMO
Radiology
29d