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

DIGITAL RADIOGRAPHY SYSTEM RADSPEED SAFIRE

K Number: K050925 · Decision Jun 1, 2005
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
49
Review Days
49

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Basic Information

Device Name
DIGITAL RADIOGRAPHY SYSTEM RADSPEED SAFIRE
K Number
K050925
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shimadzu Corp.
Date Received
April 13, 2005
Decision Date
June 1, 2005
Product Code
MQB
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
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

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