PMA P940034S006

Device
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
Applicant
Gen-Probe, Inc.
PMA number
P940034
Supplement
S006
Decision date
1997-10-30
Approval order statement
Approval for manufacturing facility relocation to 10210 Genetic Center Dr., San Diego, CA.

Current openFDA PMA Record#

Device
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
Applicant
Gen-Probe, Inc.
PMA number
P940034
Supplement
S006
Decision date
1997-10-30
Decision code
APPR
Date received
1997-09-15
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Approval for manufacturing facility relocation to 10210 Genetic Center Dr., San Diego, CA.