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PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

Page Type
Cleared 510(K)
510(k) Number
K010824
510(k) Type
Traditional
Applicant
SCIENCE INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2001
Days to Decision
78 days
Submission Type
Summary

PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

Page Type
Cleared 510(K)
510(k) Number
K010824
510(k) Type
Traditional
Applicant
SCIENCE INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2001
Days to Decision
78 days
Submission Type
Summary