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Medi-Craft , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861949SUCTION CATHETER KITOctober 22, 1986
K800507FEEDING TUBESApril 8, 1980
K800505URETHRAL CATHETERApril 8, 1980
K800508STOMACH TUBESApril 8, 1980
K800510RECTAL & HARRIS FLUSH TUBESApril 8, 1980
K800506OXYGEN CATHETERMarch 25, 1980
K800509CONNECTING TUBESMarch 25, 1980
K800504OXYGEN CONNECTING TUBESMarch 18, 1980
K800503SUCTION CATHETERMarch 18, 1980