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PAINBUSTER INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980558
510(k) Type
Traditional
Applicant
I-FLOW CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1998
Days to Decision
104 days
Submission Type
Summary

PAINBUSTER INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980558
510(k) Type
Traditional
Applicant
I-FLOW CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1998
Days to Decision
104 days
Submission Type
Summary