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RAPID DIAGNOSTIC SYSTEM FOR MYCOBACTERIUM TUBER.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871795
510(k) Type
Traditional
Applicant
GEN-PROBE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1987
Days to Decision
84 days

RAPID DIAGNOSTIC SYSTEM FOR MYCOBACTERIUM TUBER.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871795
510(k) Type
Traditional
Applicant
GEN-PROBE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1987
Days to Decision
84 days