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CUTINOVA CAVITY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952526
510(k) Type
Traditional
Applicant
BEIERSDORF, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/14/1995
Days to Decision
74 days
Submission Type
Summary

CUTINOVA CAVITY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952526
510(k) Type
Traditional
Applicant
BEIERSDORF, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/14/1995
Days to Decision
74 days
Submission Type
Summary