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SINGLE STICK RADIALLY EXPANDING DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943056
510(k) Type
Traditional
Applicant
INNERDYNE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1994
Days to Decision
92 days
Submission Type
Statement