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

COMPUTED RADDIOGRAPHY SCANNER

K Number: K102619 · Decision May 13, 2011
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
5
Review Days
242

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Basic Information

Device Name
COMPUTED RADDIOGRAPHY SCANNER
K Number
K102619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3Disc Americas
Date Received
September 13, 2010
Decision Date
May 13, 2011
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQB), ordered by most recent decision date.

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Other Clearances by 3Disc Americas

K Number Device Name
K151687 QuantorView
K133120 COMPUTED RADIOGRAPHY SCANNER
K133106 COMPUTED RADIOGRAPHY SCANNER
K131442 FIRECR DENTALIMAGING SYSTEM