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AMPLIFIED MTD (MYCOBACTERIUM TUBERCULOSIS DIRECT) TEST

FDA premarket approval P940034/S018 · decided 2010-04-23

Approval details

PMA number
P940034
Supplement
S018
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AMPLIFIED MTD (MYCOBACTERIUM TUBERCULOSIS DIRECT) TEST
Generic name
System, nucleic acid amplification, mycobacterium tuberculosis complex
Applicant
Gen-Probe, Inc.
Date received
2010-03-31
Decision date
2010-04-23
Days to decision
23 days
Decision code
OK30
Product code
MWA
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
CHANGE OF LOCATION FOR A QC LAB TO SEGREGATE THE PRE- AND POST-AMPLIFICATION STEPS INTO SEPARATE ROOMS.

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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