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SPYGLASS ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K965249
510(k) Type
Traditional
Applicant
Daig Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1997
Days to Decision
71 days
Submission Type
Summary

SPYGLASS ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K965249
510(k) Type
Traditional
Applicant
Daig Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1997
Days to Decision
71 days
Submission Type
Summary