Last synced on 9 December 2022 at 11:04 pm

STRYKER URETEROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043021
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2005
Days to Decision
133 days
Submission Type
Summary

STRYKER URETEROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043021
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2005
Days to Decision
133 days
Submission Type
Summary