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Delta III Pro

Page Type
Cleared 510(K)
510(k) Number
K221903
510(k) Type
Traditional
Applicant
Dornier Medtech America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2023
Days to Decision
237 days
Submission Type
Summary

Delta III Pro

Page Type
Cleared 510(K)
510(k) Number
K221903
510(k) Type
Traditional
Applicant
Dornier Medtech America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2023
Days to Decision
237 days
Submission Type
Summary