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Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150371
510(k) Type
Traditional
Applicant
DIROS TECHNOLOGY, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/30/2015
Days to Decision
167 days
Submission Type
Summary

Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150371
510(k) Type
Traditional
Applicant
DIROS TECHNOLOGY, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/30/2015
Days to Decision
167 days
Submission Type
Summary