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iBOT Personal Mobility Device (iBOT PMD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210920
510(k) Type
Traditional
Applicant
Mobius Mobility
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2021
Days to Decision
79 days
Submission Type
Summary

iBOT Personal Mobility Device (iBOT PMD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210920
510(k) Type
Traditional
Applicant
Mobius Mobility
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2021
Days to Decision
79 days
Submission Type
Summary