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GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST(MTD TEST)

FDA premarket approval P940034/S013 · decided 2002-01-25

Approval details

PMA number
P940034
Supplement
S013
Supplement type
Special (Immediate Track)
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST(MTD TEST)
Generic name
System, nucleic acid amplification, mycobacterium tuberculosis complex
Applicant
Gen-Probe, Inc.
Date received
2001-12-18
Decision date
2002-01-25
Days to decision
38 days
Decision code
APPR
Product code
MWA
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
APPROVAL FOR CHANGES TO THE RELATIVE LIGHT UNITS (RLU) SPECIFICATION FOR THE 0.2-0.3 MM WASHED GLASS BEADS (PART NO. 101321) AND FILLED LYSING TUBES (PART NO. 102606).

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510(k) clearances by this applicant

RecordFirmDate
APTIMA TRICHOMONAS VAGINALIS ASSAY - PANTHER (K122062)Gen-Probe, Inc.2013-01-09
APTIMA COMBO 2 ASSAY (K111409)Gen-Probe, Inc.2012-05-03
GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE MODEL#1091 (K063664)Gen-Probe, Inc.2007-01-25
GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1199 (K063451)Gen-Probe, Inc.2007-01-22
GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1091 (K062440)Gen-Probe, Inc.2006-11-07
APTIMA CT ASSAY ON THE TIGRIS DTS SYSTEM (K061413)Gen-Probe, Inc.2006-10-13
TIGRIS DTS GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1196 (K061509)Gen-Probe, Inc.2006-10-04
TIGRIS DTS GEN-PROBE APTIMA COMBO 2 ASSAY (K060652)Gen-Probe, Inc.2006-08-17