Last synced on 25 January 2026 at 3:41 am

INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE

Page Type
Cleared 510(K)
PDF
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
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