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PORTEX PERCUTANEOUS DILATATIONAL TRACHEOSTOMY KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022212
510(k) Type
Traditional
Applicant
MENTOR MEDICAL LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/21/2003
Days to Decision
256 days
Submission Type
Summary

PORTEX PERCUTANEOUS DILATATIONAL TRACHEOSTOMY KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022212
510(k) Type
Traditional
Applicant
MENTOR MEDICAL LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/21/2003
Days to Decision
256 days
Submission Type
Summary