S & W Medico Teknik - FDA 510(k) Cleared Devices
46
Total
46
Cleared
0
Denied
S & W Medico Teknik has 46 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 46 cleared submissions from 1984 to 1995. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by S & W Medico Teknik Filter by specialty or product code using the sidebar.
46 devices
Cleared
Nov 29, 1995
9267 SPO2 ATHENA MODULE
Anesthesiology
639d
Cleared
May 03, 1994
TCPO2 9260 MODULE - SYSTEM ATHENA
Anesthesiology
1030d
Cleared
Jun 29, 1993
MOD. TYPE 9230 TEMP 1 AND TEMP 2 SYSTEM ATHENA
General Hospital
609d
Cleared
Apr 09, 1993
9055 IRCA OPTION FOR SYSTEM ATHENA 9050 NT
Cardiovascular
87d
Cleared
Feb 23, 1993
9293/1 INTERFACE MODULE
Anesthesiology
225d
Cleared
Feb 05, 1993
SYSTEM ATHENA, MODIFICATION
Cardiovascular
668d
Cleared
Dec 17, 1992
VENTILATOR INTERFACE 9291/4
Anesthesiology
213d
Cleared
Oct 09, 1992
NIBP 9225 COMBI
Cardiovascular
491d
Cleared
Sep 21, 1992
TYPE INTERFACE 9271/1 INCUBATOR/WARMER
General Hospital
516d
Cleared
Jun 23, 1992
TYPE 9050/NEO
Cardiovascular
404d
Cleared
May 05, 1992
SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIA
Anesthesiology
392d
Cleared
Apr 10, 1992
PRESS 1 PRESS 2 9220 UPDATING OF THE MODULE
Cardiovascular
297d
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