Last synced on 30 September 2022 at 11:05 pm

PHEM-ALERT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012230
510(k) Type
Traditional
Applicant
FEMTEK,LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2001
Days to Decision
85 days
Submission Type
Summary

PHEM-ALERT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012230
510(k) Type
Traditional
Applicant
FEMTEK,LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2001
Days to Decision
85 days
Submission Type
Summary