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PROMEPLA INTRAVASCULAR ADMINISTRATION SET AND EXTENSION SET

Page Type
Cleared 510(K)
510(k) Number
K071421
510(k) Type
Traditional
Applicant
PROMEPLA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2007
Days to Decision
135 days
Submission Type
Summary

PROMEPLA INTRAVASCULAR ADMINISTRATION SET AND EXTENSION SET

Page Type
Cleared 510(K)
510(k) Number
K071421
510(k) Type
Traditional
Applicant
PROMEPLA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2007
Days to Decision
135 days
Submission Type
Summary