Mediflex Intl.

FDA Regulatory Profile

Mediflex Intl. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 11, 1992.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K915140PRIMARY DRESSING TRAYFebruary 11, 1992
K900841HEMODIALYSIS TRANSDUCER PROTECTORMay 15, 1990
K891077MEDIVERSE PARENTERAL NUTRITION BAGMay 24, 1989
K884243BLOOD TUBING SETDecember 8, 1988
K863496MEDIFLEX TRANSDUCER PROTECTORSeptember 23, 1986
K855039MEDIFLEX INJECTION CAPJanuary 24, 1986
K854346MEDIFLEX DISPOSABLE TUBING CLAMPNovember 18, 1985
K852106I.V. ADMINISTRATION SETJune 7, 1985
K843126MEDIFLEX DRAINAGE BAGOctober 4, 1984