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BONEE NEEDLE FOR BLADDER INJECTIONS, MODELSNBI035, NBI070

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090217
510(k) Type
Traditional
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2009
Days to Decision
84 days
Submission Type
Summary

BONEE NEEDLE FOR BLADDER INJECTIONS, MODELSNBI035, NBI070

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090217
510(k) Type
Traditional
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2009
Days to Decision
84 days
Submission Type
Summary