ClearanceBrief
Company ยท US

Conmed Andover Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1995. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRXElectrode, Electrocardiograph6
DSACable, Transducer And Electrode, Patient, (Including Connector)1
GXYElectrode, Cutaneous1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 20, 1995K9458361800 MONITORING ECG ELECTRODE AND 1870 DIAPHORETIC MONITORING ECG ELECTRODES
Conmed Andover Medical, Inc.
DRX
May 17, 1995K9462731700 MONITORING ECG ELECTRODE
Conmed Andover Medical, Inc.
DRX
Nov 22, 1994K9447261710 MONITORING ECG ELECTRODE
Conmed Andover Medical, Inc.
DRX
Nov 22, 1994K944655ECG ELECTRODE
Conmed Andover Medical, Inc.
DRX
Oct 17, 1994K9448492700 CLEARTRACE RADIOTRANSLUCENT MONITORING ECG ELECTROBE
Conmed Andover Medical, Inc.
DRX
Sep 22, 1994K942718CLOTH TENS/BNES ELECTRODE
Conmed Andover Medical, Inc.
GXY
Jul 27, 1994K941839DISPOSABLE SURGICAL CABLE
Conmed Andover Medical, Inc.
DSA
Jul 20, 1994K942925CONMED ANDOVER MED ECG ELECTRODES
Conmed Andover Medical, Inc.
DRX

Latest recalls

DateFirm and productCodeLinked 510(k)
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