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Viberect Penile Vibratory Stimulation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142304
510(k) Type
Traditional
Applicant
REFLEXONIC, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2014
Days to Decision
46 days
Submission Type
Summary

Viberect Penile Vibratory Stimulation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142304
510(k) Type
Traditional
Applicant
REFLEXONIC, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2014
Days to Decision
46 days
Submission Type
Summary