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OXYTEC, MODEL 900

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043615
510(k) Type
Traditional
Applicant
OXYTEC MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2005
Days to Decision
41 days
Submission Type
Summary

OXYTEC, MODEL 900

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043615
510(k) Type
Traditional
Applicant
OXYTEC MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2005
Days to Decision
41 days
Submission Type
Summary