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FLEXIBLE CYSTOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964037
510(k) Type
Traditional
Applicant
Applied Fiberoptics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1997
Days to Decision
135 days
Submission Type
Statement

FLEXIBLE CYSTOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964037
510(k) Type
Traditional
Applicant
Applied Fiberoptics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1997
Days to Decision
135 days
Submission Type
Statement