Medical Device Manufacturer · US , Mchenry , IL

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

11 submissions · 11 cleared · Since 1984

Total

Cleared

Denied

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

Historical record: 11 cleared submissions from 1984 to 1998. Primary specialty: Cardiovascular.

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

Qmed, 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 - Qmed, Inc.

11 devices

1-11 of 11

Cleared Dec 03, 1998

MONITOR ONE NDX

K972991 · DPS

Cardiovascular · 478d

Cleared Dec 03, 1993

PROFILOMAT

K932109 · DXN

Cardiovascular · 214d

Cleared Oct 21, 1992

INTERP-1000

K921476 · LOS

Cardiovascular · 205d

Cleared Apr 30, 1990

QEKG ELECTROCARDIOGRAPH

K897121 · DPS

Cardiovascular · 125d

Cleared Sep 30, 1987

A.R.M. (ASPEN RETURN MONITOR)

K873591 · GEI

General & Plastic Surgery · 26d

Cleared Sep 26, 1986

QMED SELF ADHERING ELECTRODE

General & Plastic Surgery · 16d

General & Plastic Surgery · 44d

Cleared Jul 27, 1984

MONITOR ONE

K841172 · DSI

Cardiovascular · 130d

Cleared Jun 19, 1984

Q-MED ELECTRODE

K840465 · DRX

Cardiovascular · 137d

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

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

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