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

FDA premarket approval P940034/S003 · decided 1996-08-22

Approval details

PMA number
P940034
Supplement
S003
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
Generic name
System, nucleic acid amplification, mycobacterium tuberculosis complex
Applicant
Gen-Probe, Inc.
Date received
1996-06-17
Decision date
1996-08-22
Days to decision
66 days
Decision code
APPR
Product code
MWA
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
APPROVAL FOR CHANGING THE PACKAGE INSERT FOR THE MTD KIT TO INCLUDE AN ADDITIONAL WARNING AND AN EXPANDED LIMITATION REGARDIGN LOW POSITIVE RESULTS WITH MOTT.

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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