FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CONTAIN(TM) LASER PLUME FILTER

K Number: K902167 · Decision Jan 4, 1991
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
7
Applicant Total
10
Review Days
234

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Basic Information

Device Name
CONTAIN(TM) LASER PLUME FILTER
K Number
K902167
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4220
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Arbor Technologies, Inc.
Date Received
May 15, 1990
Decision Date
January 4, 1991
Product Code
JDY
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
JDY Evacuator, Vapor, Cement Monomer

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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)
K890844 MICROSEPT 60/20
K874505 CONTAIN(TM)
K864113 CLYDE (TM) FILTRATION SYSTEM
K863162 VACU-GUARD