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ADULT RESECTOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890328
510(k) Type
Traditional
Applicant
CIRCON VIDEO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1990
Days to Decision
379 days

ADULT RESECTOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890328
510(k) Type
Traditional
Applicant
CIRCON VIDEO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1990
Days to Decision
379 days