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FOLATE/B12 DUO-BEAD RADIOASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822241
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1982
Days to Decision
91 days

FOLATE/B12 DUO-BEAD RADIOASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822241
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1982
Days to Decision
91 days