Medical Device Manufacturer · US , Mchenry , IL

Andover Medical, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1976

Total

Cleared

Denied

Andover Medical, Inc. has 21 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1976 to 1991.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Andover Medical, Inc.

21 devices

1-12 of 21

NORTECH MODEL 86901000 ELECTRODE

K903427 · GXY

Neurology · 17d

Cleared Jan 12, 1989

MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE

K885171 · DRO

Cardiovascular · 30d

Cleared May 09, 1986

FASTRACE III, ECG ELECTRODE

K860636 · DPS

Cardiovascular · 77d

Cleared May 08, 1986

ECG MONITORING/DEFIBRILLATION ELECTRODE

K854433 · DRX

Cardiovascular · 184d

Cleared Apr 01, 1986

UNILATERAL OXYGEN DELIVERY SYSTEM (ULODS)

FLOW-DIRECTED PEDIATRIC THERMODIL- CATH

K843410 · KRB

Cardiovascular · 81d

Cleared Nov 20, 1984

FLOW DIRECTED THERMODILUTION CATH W/VEN

K843412 · KRB

Cardiovascular · 81d

Cleared Oct 18, 1984

FLOW-DIRECTED THERMODILUTION CATH

K843409 · DYG

Cardiovascular · 48d

Cleared Oct 18, 1984

THERMAL DILUTION CATHETER

Andover Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Andover Medical, Inc.

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