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SUCTION WOUND DRAINAGE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810739
510(k) Type
Traditional
Applicant
THE UROLOGY GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1981
Days to Decision
99 days

SUCTION WOUND DRAINAGE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810739
510(k) Type
Traditional
Applicant
THE UROLOGY GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1981
Days to Decision
99 days