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AMPLIFED MYCOBACTERIUM TUBERCULOSIS DIRECTOR (MTD) TEST

FDA premarket approval P940034/S009 · decided 1998-12-01

Approval details

PMA number
P940034
Supplement
S009
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
AMPLIFED MYCOBACTERIUM TUBERCULOSIS DIRECTOR (MTD) TEST
Applicant
Gen-Probe, Inc.
Date received
1998-10-19
Decision date
1998-12-01
Days to decision
43 days
Decision code
APPR
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
Approval for additional text under Warnings: "Sediments prepared using Alpha-Tec Systems, Inc. NAC-PAC(TM) XPR-plus(TM) A.F.B. Processing Buffer have been shown to interfere with amplification."

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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