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Baxter Bentley Laboratories, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K905311 DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.DWD1991-01-15 View
510(k) K905312 DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELSDWF1991-01-15 View
510(k) K882892 MEMBRANE OXYGENATORDTZ1988-09-27 View
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