Vermont Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K030073VERMED A10021 RESTING EKG TAB ELECTRODEMarch 28, 2003
K021537MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005March 3, 2003
K010638NEUROPLUS, MODEL A10040, A10041, A10042, A10043May 3, 2001
K921498VER MED A10011 PNS DUAL ELEMENT ELECTRODEJune 9, 1993
K915831THERMAL PROBE COVERJune 8, 1992
K911687VER-MED A10020 RESTING EKG ELECTRODEOctober 10, 1991
K910139VER-MED A10014 RESTING EKG ELECTRODE & A10021August 15, 1991
K905489VER-MED A10017 UNIVERSAL ELECTRODEMarch 21, 1991
K781430PREGELLED DISPOSABLE E.K.G. ELECTRODEOctober 31, 1978