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ACCLARENT TYMPANOSTOMY TUBE AND TYMPANOSTOMY TUBE DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K103595
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2011
Days to Decision
114 days
Submission Type
Summary

ACCLARENT TYMPANOSTOMY TUBE AND TYMPANOSTOMY TUBE DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K103595
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2011
Days to Decision
114 days
Submission Type
Summary