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

Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)

K Number: K253184 · Decision Mar 25, 2026
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
1
Review Days
180

Basic Information

Device Name
Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)
K Number
K253184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4760
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zhuhai Wesee Meditech Co., Ltd.
Date Received
September 26, 2025
Decision Date
March 25, 2026
Product Code
EOB
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EOB Nasopharyngoscope (Flexible Or Rigid)

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