Prothia USA, Inc.

FDA Regulatory Profile

Prothia USA, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 8, 1983.

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