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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