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PARAGON ELECTRO. CREATINE KINASE TEST KI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802826
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1981
Days to Decision
60 days

PARAGON ELECTRO. CREATINE KINASE TEST KI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802826
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1981
Days to Decision
60 days