Last synced on 23 September 2022 at 11:05 pm

OrthoPulse

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143120
510(k) Type
Traditional
Applicant
BIOLUX RESEARCH LTD.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/24/2015
Days to Decision
267 days
Submission Type
Summary

OrthoPulse

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143120
510(k) Type
Traditional
Applicant
BIOLUX RESEARCH LTD.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/24/2015
Days to Decision
267 days
Submission Type
Summary