ClearanceBrief
Company ยท US

Vermont Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 2003. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRXElectrode, Electrocardiograph5
GXYElectrode, Cutaneous2
BXMStimulator, Nerve, Ac-Powered1
FMTWarmer, Infant Radiant1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 28, 2003K030073VERMED A10021 RESTING EKG TAB ELECTRODE
Vermont Medical, Inc.
DRX
Mar 3, 2003K021537MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005
Vermont Medical, Inc.
GXY
May 3, 2001K010638NEUROPLUS, MODEL A10040, A10041, A10042, A10043
Vermont Medical, Inc.
GXY
Jun 9, 1993K921498VER MED A10011 PNS DUAL ELEMENT ELECTRODE
Vermont Medical, Inc.
BXM
Jun 8, 1992K915831THERMAL PROBE COVER
Vermont Medical, Inc.
FMT
Oct 10, 1991K911687VER-MED A10020 RESTING EKG ELECTRODE
Vermont Medical, Inc.
DRX
Aug 15, 1991K910139VER-MED A10014 RESTING EKG ELECTRODE & A10021
Vermont Medical, Inc.
DRX
Mar 21, 1991K905489VER-MED A10017 UNIVERSAL ELECTRODE
Vermont Medical, Inc.
DRX
Oct 31, 1978K781430PREGELLED DISPOSABLE E.K.G. ELECTRODE
Vermont Medical, Inc.
DRX

Latest recalls

DateFirm and productCodeLinked 510(k)
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