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MYOVISION 3.0 WIREFREE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123399
510(k) Type
Traditional
Applicant
PRECISION BIOMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2013
Days to Decision
269 days
Submission Type
Summary

MYOVISION 3.0 WIREFREE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123399
510(k) Type
Traditional
Applicant
PRECISION BIOMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2013
Days to Decision
269 days
Submission Type
Summary