Elema-Schonander, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Elema-Schonander, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1977 to 1993. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Elema-Schonander, Inc. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Dec 15, 1993
MPQ-42
Radiology
58d
Cleared
Nov 20, 1990
SEP 90
Radiology
75d
Cleared
Sep 04, 1990
PUCK 90M
Radiology
27d
Cleared
Aug 21, 1984
SEP PROGRAMMER FOR PUCK U & UD FILMCHANG
Radiology
28d
Cleared
Aug 21, 1984
PUCK U & UD CUTFILM CHANGERS
Radiology
29d
Cleared
Feb 21, 1984
SEP PROGRAMMER SEP-M/SINGLE-PLANE &
Radiology
22d
Cleared
Oct 12, 1979
PULSE GENERATOR MODEL 637
Cardiovascular
171d
Cleared
Jun 27, 1979
PULSE GENERATOR MODEL 629
Cardiovascular
82d
Cleared
Sep 07, 1978
PULSE GENERATOR MODEL 208
Cardiovascular
59d
Cleared
Feb 24, 1977
PACEMAKER 208S
Cardiovascular
52d
Cleared
Feb 07, 1977
LEAD MODIFICATION
Cardiovascular
14d