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PAINBUSTER INFUSION KIT

Page Type
Cleared 510(K)
510(k) Number
K982946
510(k) Type
Traditional
Applicant
I-FLOW CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1998
Days to Decision
89 days
Submission Type
Summary

PAINBUSTER INFUSION KIT

Page Type
Cleared 510(K)
510(k) Number
K982946
510(k) Type
Traditional
Applicant
I-FLOW CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1998
Days to Decision
89 days
Submission Type
Summary