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RenaFlex Single-use Flexible Ureteroscope (SUURF-V Standard); RenaFlex Single-use Flexible Ureteroscope (SUURF-VR Reverse); Video System Center for Single-use Endoscopes (CV-S1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233275
510(k) Type
Traditional
Applicant
Gyrus ACMI, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2024
Days to Decision
178 days
Submission Type
Summary

RenaFlex Single-use Flexible Ureteroscope (SUURF-V Standard); RenaFlex Single-use Flexible Ureteroscope (SUURF-VR Reverse); Video System Center for Single-use Endoscopes (CV-S1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233275
510(k) Type
Traditional
Applicant
Gyrus ACMI, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2024
Days to Decision
178 days
Submission Type
Summary