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Rhinolaryngoscope system

Page Type
Cleared 510(K)
510(k) Number
K232435
510(k) Type
Traditional
Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/26/2024
Days to Decision
256 days
Submission Type
Summary

Rhinolaryngoscope system

Page Type
Cleared 510(K)
510(k) Number
K232435
510(k) Type
Traditional
Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/26/2024
Days to Decision
256 days
Submission Type
Summary