Last synced on 14 November 2025 at 11:06 pm

Unity Subcutaneous Delivery System for Remodulin

Page Type
Cleared 510(K)
510(k) Number
K190182
510(k) Type
Traditional
Applicant
DEKA Research & Development
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2019
Days to Decision
94 days
Submission Type
Summary

Unity Subcutaneous Delivery System for Remodulin

Page Type
Cleared 510(K)
510(k) Number
K190182
510(k) Type
Traditional
Applicant
DEKA Research & Development
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2019
Days to Decision
94 days
Submission Type
Summary