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PAINFUSOR CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111031
510(k) Type
Traditional
Applicant
PLAN 1 HEALTH, S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2011
Days to Decision
85 days
Submission Type
Summary

PAINFUSOR CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111031
510(k) Type
Traditional
Applicant
PLAN 1 HEALTH, S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2011
Days to Decision
85 days
Submission Type
Summary