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P.O.P. PAIN KIT

Page Type
Cleared 510(K)
510(k) Number
K001342
510(k) Type
Traditional
Applicant
POST OPERATIVE PAIN MANAGEMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/2000
Days to Decision
133 days
Submission Type
Summary

P.O.P. PAIN KIT

Page Type
Cleared 510(K)
510(k) Number
K001342
510(k) Type
Traditional
Applicant
POST OPERATIVE PAIN MANAGEMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/2000
Days to Decision
133 days
Submission Type
Summary