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STRYKER FLEXIBLE CYSTONEPHROSCOPE

Page Type
Cleared 510(K)
510(k) Number
K043022
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2005
Days to Decision
132 days
Submission Type
Summary

STRYKER FLEXIBLE CYSTONEPHROSCOPE

Page Type
Cleared 510(K)
510(k) Number
K043022
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2005
Days to Decision
132 days
Submission Type
Summary