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

Laser Speckle Imaging System (RFLSI CZW)

K Number: K233076 · Decision May 28, 2024
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
47
Applicant Total
1
Review Days
245

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Basic Information

Device Name
Laser Speckle Imaging System (RFLSI CZW)
K Number
K233076
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rwd Life Science Co., Ltd.
Date Received
September 26, 2023
Decision Date
May 28, 2024
Product Code
DPT
Advisory Committee
Cardiovascular
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPT Probe, Blood-Flow, Extravascular

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