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SURGITEK NEPHROSTENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831446
510(k) Type
Traditional
Applicant
MEC/SURGITEK PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1983
Days to Decision
48 days

SURGITEK NEPHROSTENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831446
510(k) Type
Traditional
Applicant
MEC/SURGITEK PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1983
Days to Decision
48 days