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ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883609
510(k) Type
Traditional
Applicant
SQUIBB DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1989
Days to Decision
235 days

ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883609
510(k) Type
Traditional
Applicant
SQUIBB DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1989
Days to Decision
235 days