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Prothia USA, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K831071UNIVERSAL INSTRU. SET FOR NEUROVASCULARJune 8, 1983
K830993AMPLIGREFFEMay 3, 1983
K823581ELPHA 500March 24, 1983
K830058MYOGRAPH 2000March 7, 1983
K823583MYOTEST NERVE STIMULATORDecember 30, 1982