Atlas FDA

T SPOT-TB TEST

FDA premarket approval P070006/S025 · decided 2024-06-25

Approval details

PMA number
P070006
Supplement
S025
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
T SPOT-TB TEST
Generic name
Mycobacterium tuberculosis, Cell mediated immune response, enzyme-linked immunospot test
Applicant
Oxford Immunotec, Ltd.
Date received
2024-05-29
Decision date
2024-06-25
Days to decision
27 days
Decision code
OK30
Product code
OJN
Advisory committee
Microbiology
Expedited review
No
Location
Milton Park, Abingdon Oxfordshire
Statement
to update QC testing for a process

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