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Unoplast A/S

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K896734FEEDING TUBEDecember 21, 1990
K896729NELATON-, FEMALE - OR TIEMANN CATHETERNovember 5, 1990
K896732UNOMETER 500November 2, 1990
K896730SUCTION CATHETER STRAIGHT/COUDEMarch 30, 1990
K896731OXYGEN CATHETERSMarch 30, 1990
K896733VACCONFebruary 1, 1990
K802248DISARP ORIGINALSeptember 26, 1980