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MODULAR ENDOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093785
510(k) Type
Traditional
Applicant
SIALO TECHNOLOGY, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/18/2010
Days to Decision
252 days
Submission Type
Summary