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LEGIONELLA DIRECT FLUORESCENT ANTIBODY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812006
510(k) Type
Traditional
Applicant
CENTERS FOR DISEASE CONTROL AND PREVENTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1981
Days to Decision
54 days

LEGIONELLA DIRECT FLUORESCENT ANTIBODY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812006
510(k) Type
Traditional
Applicant
CENTERS FOR DISEASE CONTROL AND PREVENTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1981
Days to Decision
54 days