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

ExamVue Duo

K Number: K213057 · Decision Feb 18, 2022
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
9
Review Days
149

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Basic Information

Device Name
ExamVue Duo
K Number
K213057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jpi Healthcare Co, Ltd.
Date Received
September 22, 2021
Decision Date
February 18, 2022
Product Code
KPR
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
KPR System, X-Ray, Stationary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPR), ordered by most recent decision date.

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Other Clearances by Jpi Healthcare Co, Ltd.

K Number Device Name
K260482 DRE Duo
K244010 ExamVue Apex
K142930 Exam Vue DR
K102327 CLEARVISION DR 7000F
K101779 CLEARVISION DR 2000 DIGITAL RADIOGRAPHY X-RAY SYSTEM
K955706 JPI AUTOMATIC X-RAY FILM PROCESSOR
K954161 JPI INTENSIFYING SCREEN
K950043 JPI AUTOMATIC X-RAY FILM PROCESSOR