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INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990854
510(k) Type
Traditional
Applicant
INNERDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1999
Days to Decision
140 days
Submission Type
Summary

INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990854
510(k) Type
Traditional
Applicant
INNERDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1999
Days to Decision
140 days
Submission Type
Summary