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Navigator (FMNVG15); Navigator XL (FMNVX06)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240105
510(k) Type
Traditional
Applicant
Forcemech International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2024
Days to Decision
226 days
Submission Type
Summary

Navigator (FMNVG15); Navigator XL (FMNVX06)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240105
510(k) Type
Traditional
Applicant
Forcemech International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2024
Days to Decision
226 days
Submission Type
Summary