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ACCLARENT SE Inflation Device

Page Type
Cleared 510(K)
510(k) Number
K150172
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2015
Days to Decision
71 days
Submission Type
Summary

ACCLARENT SE Inflation Device

Page Type
Cleared 510(K)
510(k) Number
K150172
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2015
Days to Decision
71 days
Submission Type
Summary