FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

AERODR X70

K Number: K121109 · Decision May 23, 2012
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
27
Review Days
41

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Basic Information

Device Name
AERODR X70
K Number
K121109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Konica Minolta Medical & Graphic, Inc.
Date Received
April 12, 2012
Decision Date
May 23, 2012
Product Code
KPR
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
KPR System, X-Ray, Stationary

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Other Clearances by Konica Minolta Medical & Graphic, Inc.

K Number Device Name
K130936 AERODR SYSTEM WITH P-31
K123499 AEROPILOT
K120752 AERODR STITCHING SYSTEM
K120477 AEROSYNC FOR AERODR SYSTEM
K120131 REGIUS SIGMA2
K113248 AERODR SYSTEM WITH P-21
K110717 KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM
K103703 REGUIS SIGMA
K101842 ACIES
K102349 AERODR SYSTEM
Search all 27 clearances from Konica Minolta Medical & Graphic, Inc. →