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ARTERIAL ANCHOR BANDAGE

Page Type
Cleared 510(K)
510(k) Number
K883957
510(k) Type
Traditional
Applicant
GUIDELINES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1988
Days to Decision
29 days

ARTERIAL ANCHOR BANDAGE

Page Type
Cleared 510(K)
510(k) Number
K883957
510(k) Type
Traditional
Applicant
GUIDELINES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1988
Days to Decision
29 days