Medical Device Manufacturer · US , Mchenry , IL

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

11 submissions · 11 cleared · Since 1979

Total

Cleared

Denied

Alimed, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1979 to 1996. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Alimed, Inc. Filter by specialty or product code using the sidebar.

Alimed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Alimed, Inc.

11 devices

1-11 of 11

Cleared Oct 31, 1996

UNIVERSAL ECONO-STRAP, QUALCRAFT UNIVERSAL STRAPS

K963527 · FMQ

General Hospital · 57d

Cleared Oct 29, 1996

ALIMED POSITIONING 7 SAFETY STRAPS (THREE TYPES), UNIVERSAL CR/MRI WIDE BODY...

K963528 · FMQ

General Hospital · 55d

Cleared Oct 28, 1996

STRAP WEDGE

K963526 · FMQ

General Hospital · 54d

Cleared Feb 18, 1992

MINI VIBRATOR

K920487 · IRO

Physical Medicine · 19d

Cleared Mar 23, 1984

PROTECTA COAT SPONGES

General Hospital · 28d

Cleared Sep 17, 1982

TOTAL FINGER FLEXION SPLINT

K822651 · ILH

Physical Medicine · 15d

Cleared Apr 15, 1982

ARTERIAL CANALIZATION DEVICE

Physical Medicine · 13d

Cleared Aug 07, 1980

PLASTAZOTE SHOE

K801743 · KNP

Physical Medicine · 10d

Cleared Jul 17, 1979

ECHO CARDIOGRAM PAD

K791189 · FNJ

General Hospital · 21d

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

FDA 510(k) Regulatory Record - Alimed, Inc.

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