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

Digital Flat Panel X-ray Detector (1717WCE, 1717WCE-HR, 1717WCE-HS, 1717WCE-GF)

K Number: K242394 · Decision Sep 9, 2024
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
38
Review Days
27

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Basic Information

Device Name
Digital Flat Panel X-ray Detector (1717WCE, 1717WCE-HR, 1717WCE-HS, 1717WCE-GF)
K Number
K242394
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rayence Co., Ltd.
Date Received
August 13, 2024
Decision Date
September 9, 2024
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 Rayence Co., Ltd.

K Number Device Name
K243849 2430TCA with Xmaru W
K240371 0909FCC, 0909FCC-HS
K231467 1417WCE, 1417WCE-HR, 1417WCE-HS, 1417WCE-GF
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. →