Andover Medical, Inc. is one of 6920 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Andover Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CANMED 451, NORTECH MODEL 86901000 ELECTRODE, MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE
21
Total
21
Cleared
0
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
Cleared
Feb 07, 1991
CANMED 451
Cardiovascular
45d
Cleared
Aug 17, 1990
NORTECH MODEL 86901000 ELECTRODE
Neurology
17d
Cleared
Jan 12, 1989
MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE
Cardiovascular
30d
Cleared
May 09, 1986
FASTRACE III, ECG ELECTRODE
Cardiovascular
77d
Cleared
May 08, 1986
ECG MONITORING/DEFIBRILLATION ELECTRODE
Cardiovascular
184d
Cleared
Apr 01, 1986
UNILATERAL OXYGEN DELIVERY SYSTEM (ULODS)
Anesthesiology
48d
Cleared
Mar 31, 1986
AMI CARDIO-PAD
Cardiovascular
62d
Cleared
Nov 20, 1984
FLOW-DIRECTED PEDIATRIC THERMODIL- CATH
Cardiovascular
81d
Cleared
Nov 20, 1984
FLOW DIRECTED THERMODILUTION CATH W/VEN
Cardiovascular
81d
Cleared
Oct 18, 1984
FLOW-DIRECTED THERMODILUTION CATH
Cardiovascular
48d
Cleared
Oct 18, 1984
THERMAL DILUTION CATHETER
Cardiovascular
48d
Cleared
Jun 30, 1983
NEURO EASE
Neurology
27d