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P.O.P. PAIN KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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