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TYMPANOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K082188
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2008
Days to Decision
46 days
Submission Type
Summary

TYMPANOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K082188
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2008
Days to Decision
46 days
Submission Type
Summary