Last synced on 25 January 2026 at 3:41 am

JMD AV FISTULA NEEDLE (MODIFICATION)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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