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HiTop® (Models: HiToP®4touch, HiToP®2touch, HiToP®1touch)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213655
510(k) Type
Traditional
Applicant
HillTek LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2023
Days to Decision
424 days
Submission Type
Summary

HiTop® (Models: HiToP®4touch, HiToP®2touch, HiToP®1touch)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213655
510(k) Type
Traditional
Applicant
HillTek LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2023
Days to Decision
424 days
Submission Type
Summary