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CELON ENT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032838
510(k) Type
Traditional
Applicant
Celon AG Medical Instruments
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/26/2003
Days to Decision
15 days
Submission Type
Summary

CELON ENT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032838
510(k) Type
Traditional
Applicant
Celon AG Medical Instruments
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/26/2003
Days to Decision
15 days
Submission Type
Summary