Last synced on 14 November 2025 at 11:06 pm

ENTELLUS MEDICAL BALLOON DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093007
510(k) Type
Traditional
Applicant
Entellus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2010
Days to Decision
130 days
Submission Type
Summary

ENTELLUS MEDICAL BALLOON DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093007
510(k) Type
Traditional
Applicant
Entellus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2010
Days to Decision
130 days
Submission Type
Summary