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GEN-PROBE (R) LUMINOMETER - LEADER (TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872219
510(k) Type
Traditional
Applicant
GEN-PROBE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1987
Days to Decision
70 days

GEN-PROBE (R) LUMINOMETER - LEADER (TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872219
510(k) Type
Traditional
Applicant
GEN-PROBE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1987
Days to Decision
70 days