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LUNETTE MENSTRUAL CUP, MODELS 1 AND 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091754
510(k) Type
Traditional
Applicant
LUNE GROUP LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2009
Days to Decision
150 days
Submission Type
Summary

LUNETTE MENSTRUAL CUP, MODELS 1 AND 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091754
510(k) Type
Traditional
Applicant
LUNE GROUP LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2009
Days to Decision
150 days
Submission Type
Summary