ClearanceBrief
Company ยท US

Arbor Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1997. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BSNFilter, Conduction, Anesthetic2
FPBFilter, Infusion Line2
GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered2
CAKMicrofilter, Blood Transfusion1
HIFInsufflator, Laparoscopic1
JDYEvacuator, Vapor, Cement Monomer1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 4, 1997K960928SYRINGEFILTER
Arbor Technologies, Inc.
BSN
Jan 22, 1997K964283AUTOPRIME
Arbor Technologies, Inc.
FPB
Mar 22, 1994K922777PRESSURE TUBING AND ACCESSORIES
Arbor Technologies, Inc.
HIF
Apr 23, 1991K902666ANESTHESIA CONDUCTION FILTER
Arbor Technologies, Inc.
BSN
Feb 7, 1991K895859CONTAIN(TM)
Arbor Technologies, Inc.
GCX
Jan 4, 1991K902167CONTAIN(TM) LASER PLUME FILTER
Arbor Technologies, Inc.
JDY
Jun 7, 1989K890844MICROSEPT 60/20
Arbor Technologies, Inc.
CAK
May 20, 1988K874505CONTAIN(TM)
Arbor Technologies, Inc.
GCX
Feb 4, 1987K864113CLYDE (TM) FILTRATION SYSTEM
Arbor Technologies, Inc.
FPB
Aug 29, 1986K863162VACU-GUARD
Arbor Technologies, Inc.

Latest recalls

DateFirm and productCodeLinked 510(k)
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