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
K800510RECTAL & HARRIS FLUSH TUBESApril 8, 1980
K800505URETHRAL CATHETERApril 8, 1980
K800507FEEDING TUBESApril 8, 1980
K800508STOMACH TUBESApril 8, 1980
K800509CONNECTING TUBESMarch 25, 1980
K800506OXYGEN CATHETERMarch 25, 1980
K800503SUCTION CATHETERMarch 18, 1980
K800504OXYGEN CONNECTING TUBESMarch 18, 1980