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PER-FIT PERCUTANEOUS TRACHEOSTOMY KIT W/PORTEX TRACHEOSTMY TUBE & DISP. INNER CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960429
510(k) Type
Traditional
Applicant
SMITHS INDUSTRIES MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/2/1996
Days to Decision
92 days
Submission Type
Summary

PER-FIT PERCUTANEOUS TRACHEOSTOMY KIT W/PORTEX TRACHEOSTMY TUBE & DISP. INNER CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960429
510(k) Type
Traditional
Applicant
SMITHS INDUSTRIES MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/2/1996
Days to Decision
92 days
Submission Type
Summary