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CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951972
510(k) Type
Traditional
Applicant
CABOT MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1995
Days to Decision
85 days
Submission Type
Statement

CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951972
510(k) Type
Traditional
Applicant
CABOT MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1995
Days to Decision
85 days
Submission Type
Statement