FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CONTAIN(TM)

K Number: K874505 · Decision May 20, 1988
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
10
Review Days
200

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Basic Information

Device Name
CONTAIN(TM)
K Number
K874505
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Arbor Technologies, Inc.
Date Received
November 2, 1987
Decision Date
May 20, 1988
Product Code
GCX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

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Other Clearances by Arbor Technologies, Inc.

K Number Device Name
K960928 SYRINGEFILTER
K964283 AUTOPRIME
K922777 PRESSURE TUBING AND ACCESSORIES
K902666 ANESTHESIA CONDUCTION FILTER
K895859 CONTAIN(TM)
K902167 CONTAIN(TM) LASER PLUME FILTER
K890844 MICROSEPT 60/20
K864113 CLYDE (TM) FILTRATION SYSTEM
K863162 VACU-GUARD