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THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011210
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2001
Days to Decision
118 days
Submission Type
Summary

THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011210
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2001
Days to Decision
118 days
Submission Type
Summary