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

.DECIMAL APERTURE

K Number: K071077 · Decision May 18, 2007
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
50
Applicant Total
9
Review Days
31

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Basic Information

Device Name
.DECIMAL APERTURE
K Number
K071077
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
.Decimal, Inc.
Date Received
April 17, 2007
Decision Date
May 18, 2007
Product Code
IXI
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IXI Block, Beam-Shaping, Radiation Therapy

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K091911 BOLUS COMPENSATOR
K083672 P.D SOFTWARE
K071078 .DECIMAL RANGE COMPENSATOR
K061440 P.D