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RADIONUCLIDE INFUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842568
510(k) Type
Traditional
Applicant
SQUIBB DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1984
Days to Decision
109 days

RADIONUCLIDE INFUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842568
510(k) Type
Traditional
Applicant
SQUIBB DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1984
Days to Decision
109 days