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PERCUTANEOUS TRACHEOSTOMY TUBE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931611
510(k) Type
Traditional
Applicant
CRANDALL MEDICAL DEVICES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
8/27/1993
Days to Decision
148 days
Submission Type
Statement

PERCUTANEOUS TRACHEOSTOMY TUBE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931611
510(k) Type
Traditional
Applicant
CRANDALL MEDICAL DEVICES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
8/27/1993
Days to Decision
148 days
Submission Type
Statement