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

1417WCE, 1417WCE-HR, 1417WCE-HS, 1417WCE-GF

K Number: K231467 · Decision Jun 21, 2023
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
38
Review Days
30

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Basic Information

Device Name
1417WCE, 1417WCE-HR, 1417WCE-HS, 1417WCE-GF
K Number
K231467
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 22, 2023
Decision Date
June 21, 2023
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
K220689 Vatech Clismile
K212753 0909FCB, 1212FCA
K202902 2430MCA with Xmaru W
K210985 1717FCC
K202722 1212FCA
K201796 1717SCV, 1717SGV
K190866 XmaruView V1 (Xmaru Chiroview, Xmaru Podview)
Search all 38 clearances from Rayence Co., Ltd. →