Elmed, Inc. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Elmed, Inc. has 26 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 26 cleared submissions from 1977 to 2001.
Browse the FDA 510(k) cleared devices submitted by Elmed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Elmed, Inc.
26 devices
Cleared
May 14, 2001
DENSTAT
General & Plastic Surgery
87d
Cleared
Mar 19, 1998
ELMED ESU 120 M/M DIGITAL
General & Plastic Surgery
87d
Cleared
Jan 18, 1996
ELMED RF-ALERT
General & Plastic Surgery
189d
Cleared
Aug 14, 1995
ELMED THERMO-FLUX
General & Plastic Surgery
101d
Cleared
Nov 15, 1994
ELMED LBC 50-P
Obstetrics & Gynecology
685d
Cleared
May 02, 1994
ELMED ESU 300 M/M AND DIGITAL
General & Plastic Surgery
320d
Cleared
May 17, 1993
ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/M
General & Plastic Surgery
399d
Cleared
Nov 05, 1992
ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL
General & Plastic Surgery
321d
Cleared
Jan 31, 1991
ELMED PNEUMOMAT DIGITAL
Obstetrics & Gynecology
58d
Cleared
Apr 16, 1990
SIEMENS STEREODYNATOR 828
Physical Medicine
741d
Cleared
Mar 10, 1988
SIEMENS NEUROTON 826 AND 827
Physical Medicine
79d
Cleared
Jan 13, 1988
SIEMENS SONODYNATOR 834, ULTRASOUND/STIMULATION
Physical Medicine
173d