FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Tuxedo Digital Dental Sensor

K Number: K153710 · Decision Mar 18, 2016
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
3
Review Days
85

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Basic Information

Device Name
Tuxedo Digital Dental Sensor
K Number
K153710
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Led Dental, Inc.
Date Received
December 24, 2015
Decision Date
March 18, 2016
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 Led Dental, Inc.

K Number Device Name
K102083 VELSCOPE VX
K070523 MODIFICATION TO: VELSCOPE