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Baxter Bentley Laboratories, Inc.

FDA Regulatory Profile

Baxter Bentley Laboratories, Inc. 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 January 15, 1991.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.January 15, 1991
K905312DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELSJanuary 15, 1991
K882892MEMBRANE OXYGENATORSeptember 27, 1988

FDA data resources