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VIVAMED FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K903440
510(k) Type
Traditional
Applicant
S.S. ENT.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1992
Days to Decision
629 days

VIVAMED FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K903440
510(k) Type
Traditional
Applicant
S.S. ENT.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1992
Days to Decision
629 days