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ProntoPump Sterile Tube Set

Page Type
Cleared 510(K)
510(k) Number
K200893
510(k) Type
Traditional
Applicant
IPAX, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2021
Days to Decision
396 days
Submission Type
Summary

ProntoPump Sterile Tube Set

Page Type
Cleared 510(K)
510(k) Number
K200893
510(k) Type
Traditional
Applicant
IPAX, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2021
Days to Decision
396 days
Submission Type
Summary