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REPRO-MED SYSTEMS INFUSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844401
510(k) Type
Traditional
Applicant
REPRO-MED SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1985
Days to Decision
119 days

REPRO-MED SYSTEMS INFUSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844401
510(k) Type
Traditional
Applicant
REPRO-MED SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1985
Days to Decision
119 days