FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Imaging Plate Scanner, i-Scan

K Number: K212080 · Decision Sep 27, 2021
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
14
Review Days
87

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Basic Information

Device Name
Imaging Plate Scanner, i-Scan
K Number
K212080
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guilin Woodpecker Medical Instrument Co., Ltd.
Date Received
July 2, 2021
Decision Date
September 27, 2021
Product Code
MUH
Advisory Committee
Dental
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
MUH System, X-Ray, Extraoral Source, Digital

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