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GASTROINTESTINAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K851671
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1985
Days to Decision
52 days

GASTROINTESTINAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K851671
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1985
Days to Decision
52 days