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PERCUTANEOUS TRACHEOSTOMY TUBE KIT

Page Type
Cleared 510(K)
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)
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