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ENDOTRACHEAL TUBE, ACCESSORY

Page Type
Cleared 510(K)
510(k) Number
K862347
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1986
Days to Decision
21 days

ENDOTRACHEAL TUBE, ACCESSORY

Page Type
Cleared 510(K)
510(k) Number
K862347
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1986
Days to Decision
21 days