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

1417WGC_127um and 1417WGC_140um

K Number: K171417 · Decision Jun 12, 2017
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
418
Applicant Total
16
Review Days
28

Basic Information

Device Name
1417WGC_127um and 1417WGC_140um
K Number
K171417
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rayence Co., Ltd
Date Received
May 15, 2017
Decision Date
June 12, 2017
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 Rayence Co., Ltd

K Number Device Name
K243849 2430TCA with Xmaru W
K242394 Digital Flat Panel X-ray Detector (1717WCE, 1717WCE-HR, 1717WCE-HS, 1717WCE-GF)
K240371 0909FCC, 0909FCC-HS
K231467 1417WCE, 1417WCE-HR, 1417WCE-HS, 1417WCE-GF
K212753 0909FCB, 1212FCA
K202902 2430MCA with Xmaru W
K210985 1717FCC
K202722 1212FCA
K190866 XmaruView V1 (Xmaru Chiroview, Xmaru Podview)
K171418 1417WCC_127um and1417WCC_140um
Search all 16 clearances from Rayence Co., Ltd →