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

LASER IMAGER DRYPRO MODEL 873

K Number: K081637 · Decision Jul 1, 2008
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
120
Applicant Total
27
Review Days
20

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Basic Information

Device Name
LASER IMAGER DRYPRO MODEL 873
K Number
K081637
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2040
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Konica Minolta Medical & Graphic, Inc.
Date Received
June 11, 2008
Decision Date
July 1, 2008
Product Code
LMC
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
LMC Camera, Multi Format, Radiological

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K103703 REGUIS SIGMA
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