Medical Device Manufacturer · US , Mchenry , IL

Elmed, Inc. - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 1977

Total

Cleared

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) Regulatory Record - Elmed, Inc.

26 devices

1-12 of 26

Cleared May 14, 2001

DENSTAT

K010465 · GEI

General & Plastic Surgery · 87d

Cleared Mar 19, 1998

ELMED ESU 120 M/M DIGITAL

K974793 · GEI

General & Plastic Surgery · 87d

Cleared Jan 18, 1996

ELMED RF-ALERT

K953271 · GEI

General & Plastic Surgery · 189d

Cleared Aug 14, 1995

ELMED THERMO-FLUX

K952110 · GEI

General & Plastic Surgery · 101d

Cleared Nov 15, 1994

ELMED LBC 50-P

K926517 · HIN

Obstetrics & Gynecology · 685d

Cleared May 02, 1994

ELMED ESU 300 M/M AND DIGITAL

K932938 · GEI

General & Plastic Surgery · 320d

Cleared May 17, 1993

ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/M

K921770 · GEI

General & Plastic Surgery · 399d

Cleared Nov 05, 1992

ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL

K915731 · GEI

General & Plastic Surgery · 321d

Cleared Jan 31, 1991

ELMED PNEUMOMAT DIGITAL

K905417 · HIF

Obstetrics & Gynecology · 58d

Cleared Apr 16, 1990

SIEMENS STEREODYNATOR 828

K881431 · IPF

Physical Medicine · 741d

Cleared Mar 10, 1988

SIEMENS NEUROTON 826 AND 827

K875238 · IPF

Physical Medicine · 79d

Cleared Jan 13, 1988

SIEMENS SONODYNATOR 834, ULTRASOUND/STIMULATION

K872909 · IMG

Physical Medicine · 173d

Elmed, Inc. - FDA 510(k) Cleared Devices

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