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Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241028
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2024
Days to Decision
102 days
Submission Type
Summary

Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241028
510(k) Type
Traditional
Applicant
Coloplast
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2024
Days to Decision
102 days
Submission Type
Summary