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SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031553
510(k) Type
Traditional
Applicant
ARCADIA MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2003
Days to Decision
183 days
Submission Type
Summary

SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031553
510(k) Type
Traditional
Applicant
ARCADIA MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2003
Days to Decision
183 days
Submission Type
Summary