Atlas FDA

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

FDA premarket approval P940034/S006 · decided 1997-10-30

Approval details

PMA number
P940034
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
Applicant
Gen-Probe, Inc.
Date received
1997-09-15
Decision date
1997-10-30
Days to decision
45 days
Decision code
APPR
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
Approval for manufacturing facility relocation to 10210 Genetic Center Dr., San Diego, CA.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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