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STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001961
510(k) Type
Abbreviated
Applicant
Stoeckert Instrumente
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2001
Days to Decision
212 days
Submission Type
Summary

STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001961
510(k) Type
Abbreviated
Applicant
Stoeckert Instrumente
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2001
Days to Decision
212 days
Submission Type
Summary