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RECTAL TUBE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K760886
510(k) Type
Traditional
Applicant
VAN SICKLE PLASTICS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1976
Days to Decision
48 days

RECTAL TUBE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K760886
510(k) Type
Traditional
Applicant
VAN SICKLE PLASTICS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1976
Days to Decision
48 days