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JMD AV FISTULA NEEDLE (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K860789
510(k) Type
Traditional
Applicant
JMS CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/18/1986
Days to Decision
20 days

JMD AV FISTULA NEEDLE (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K860789
510(k) Type
Traditional
Applicant
JMS CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/18/1986
Days to Decision
20 days