Medical Device Manufacturer · US , Bellows Falls , VT

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

9 submissions · 9 cleared · Since 1978

Total

Cleared

Denied

Vermont Medical, Inc. has 9 FDA 510(k) cleared medical devices. Based in Bellows Falls, US.

Historical record: 9 cleared submissions from 1978 to 2003. Primary specialty: Cardiovascular.

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

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

9 devices

1-9 of 9

Cleared Mar 28, 2003

VERMED A10021 RESTING EKG TAB ELECTRODE

K030073 · DRX

Cardiovascular · 79d

Cleared Mar 03, 2003

MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005

K021537 · GXY

Neurology · 297d

Cleared May 03, 2001

NEUROPLUS, MODEL A10040, A10041, A10042, A10043

K010638 · GXY

Neurology · 59d

Cleared Jun 09, 1993

VER MED A10011 PNS DUAL ELEMENT ELECTRODE

K921498 · BXM

Anesthesiology · 435d

Cleared Jun 08, 1992

THERMAL PROBE COVER

K915831 · FMT

General Hospital · 161d

Cleared Oct 10, 1991

VER-MED A10020 RESTING EKG ELECTRODE

K911687 · DRX

Cardiovascular · 177d

Cleared Aug 15, 1991

VER-MED A10014 RESTING EKG ELECTRODE & A10021

K910139 · DRX

Cardiovascular · 213d

Cleared Mar 21, 1991

VER-MED A10017 UNIVERSAL ELECTRODE

K905489 · DRX

Cardiovascular · 104d

Cleared Oct 31, 1978

PREGELLED DISPOSABLE E.K.G. ELECTRODE

K781430 · DRX

Cardiovascular · 71d

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

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