FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Pixx2430 Digital Diagnostic X-Ray Receptor Panel

K Number: K190691 · Decision Apr 4, 2019
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
4
Review Days
17

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Basic Information

Device Name
Pixx2430 Digital Diagnostic X-Ray Receptor Panel
K Number
K190691
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pixxgen Corporation
Date Received
March 18, 2019
Decision Date
April 4, 2019
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 Pixxgen Corporation

K Number Device Name
K211108 Prudent 1717, Prudent 1417, Prudent 1212
K182533 PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels
K180976 PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels