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SabreLine and SabreGuard Laser Fibers

Page Type
Cleared 510(K)
510(k) Number
K182831
510(k) Type
Traditional
Applicant
Coloplast Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2018
Days to Decision
62 days
Submission Type
Summary

SabreLine and SabreGuard Laser Fibers

Page Type
Cleared 510(K)
510(k) Number
K182831
510(k) Type
Traditional
Applicant
Coloplast Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2018
Days to Decision
62 days
Submission Type
Summary