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MEDEX 3000 SERIES SYRINGE INFUSION PUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982640
510(k) Type
Traditional
Applicant
MEDEX, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
4/6/1999
Days to Decision
251 days

MEDEX 3000 SERIES SYRINGE INFUSION PUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982640
510(k) Type
Traditional
Applicant
MEDEX, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
4/6/1999
Days to Decision
251 days