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SIALO BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072749
510(k) Type
Traditional
Applicant
SIALO TECHNOLOGY, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
5/14/2008
Days to Decision
230 days
Submission Type
Summary