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Metronic, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K031210MODEL 4951M MYOCARDIAL UNIPOLAR LEADMay 16, 2003
K911827MODEL 5866-9M & MODEL 6981MJuly 23, 1991
K874884MEDTRONIC(R) ORTHOFLEX(TM)January 28, 1988
K832505IMAGE PROCESSING SYS A3September 12, 1983