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MODIFICATION OF JMS NEEDLES AND JMS SYRINGES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991904
510(k) Type
Traditional
Applicant
JMS CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/31/1999
Days to Decision
88 days
Submission Type
Statement

MODIFICATION OF JMS NEEDLES AND JMS SYRINGES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991904
510(k) Type
Traditional
Applicant
JMS CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/31/1999
Days to Decision
88 days
Submission Type
Statement