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FDA 510(k) Applications Submitted by VERMONT MEDICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030073
01/08/2003
VERMED A10021 RESTING EKG TAB ELECTRODE
VERMONT MEDICAL, INC.
K010638
03/05/2001
NEUROPLUS, MODEL A10040, A10041, A10042, A10043
VERMONT MEDICAL, INC.
K021537
05/10/2002
MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005
VERMONT MEDICAL, INC.
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