Last synced on 19 July 2024 at 11:05 pm

HD Mediastinoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202272
510(k) Type
Traditional
Applicant
Karl Storz Endoscopy America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2021
Days to Decision
273 days
Submission Type
Summary

HD Mediastinoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202272
510(k) Type
Traditional
Applicant
Karl Storz Endoscopy America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2021
Days to Decision
273 days
Submission Type
Summary