Last synced on 14 November 2025 at 11:06 pm

CELON ENT SYSTEM

Page Type
Cleared 510(K)
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)
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