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Jostra Bentley

FDA Regulatory Profile

Jostra Bentley appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 20, 1999.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992559HOLLOW FIBER MEMBRANE OYGENATOR QUADROX HMO 1010September 20, 1999
K984338JOSTRA HL-20 TWIN PUMPAugust 19, 1999
K945720JOSTRA HL-15 MODULAR HEART-LUNG MACHINE (HEREINAFTER CALLED THE HL-15 OR THE DEVICEMarch 29, 1995

FDA data resources