Euro-Med Intl.

FDA Regulatory Profile

Euro-Med Intl. appears in FDA public data with 0 recalls, 16 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 5, 1988.

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K883884PROSTATIC CORE-CUT NEEDLEDecember 5, 1988
K882404KEVOR-CURETTEJuly 8, 1988
K854901PACIFIC GRASPERMay 2, 1986
K854898ATLANTIC GRASPERMay 2, 1986
K854896HOOK SCISSORMay 2, 1986
K854894SPOONMay 2, 1986
K854890HOOK PROBEMay 2, 1986
K854895BASKET FORCEPMay 2, 1986
K854891KNIFEMay 2, 1986
K854897MAX-I-GRASPMay 2, 1986
K854889FLEX-I-GRASPFebruary 21, 1986
K854888RANDALL CURETTEDecember 24, 1985
K854893KEYES SKIN PUNCHDecember 24, 1985
K854892RULERDecember 24, 1985
K854899NOVAK CURETTEDecember 24, 1985
K854900EPISIOTOMY SCISSORSDecember 24, 1985