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

SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB

K Number: K101289 · Decision Aug 3, 2010
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
18
Review Days
88

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Basic Information

Device Name
SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB
K Number
K101289
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Air Techniques, Inc.
Date Received
May 7, 2010
Decision Date
August 3, 2010
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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Other Clearances by Air Techniques, Inc.

K Number Device Name
K191623 ScanX Touch/ScanX Duo Touch
K190949 ScanX Barrier Envelopes
K090169 SPECTRA FLUORESCENCE CARIES DETECTION DEVICE
K052271 RINSENDO
K050693 ACCENT
K042397 SCANX 14
K042266 ACCLAIM
K031198 SCANX 10
K024285 A/T X-RAY 70
K013893 SCANX
Search all 18 clearances from Air Techniques, Inc. →