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VISITEC NEEDLE RANGE (ORTHOPAEDIC)

Page Type
Cleared 510(K)
510(k) Number
K811961
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1981
Days to Decision
10 days

VISITEC NEEDLE RANGE (ORTHOPAEDIC)

Page Type
Cleared 510(K)
510(k) Number
K811961
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1981
Days to Decision
10 days