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LAPORT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092584
510(k) Type
Traditional
Applicant
MGB ENDOSKOPISCHE GERATE GMBH (BERLIN)
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/22/2010
Days to Decision
210 days
Submission Type
Statement