Last synced on 16 August 2024 at 11:05 pm

Single-use Flexible Rhinolaryngoscope; Digital Video Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230536
510(k) Type
Traditional
Applicant
Hunan Vathin Medical Instrument Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/14/2023
Days to Decision
107 days
Submission Type
Summary

Single-use Flexible Rhinolaryngoscope; Digital Video Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230536
510(k) Type
Traditional
Applicant
Hunan Vathin Medical Instrument Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/14/2023
Days to Decision
107 days
Submission Type
Summary