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LAGIS ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090309
510(k) Type
Traditional
Applicant
Lagis Enterprises Co, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2009
Days to Decision
203 days
Submission Type
Summary

LAGIS ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090309
510(k) Type
Traditional
Applicant
Lagis Enterprises Co, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2009
Days to Decision
203 days
Submission Type
Summary