Atlas FDA

T-SPOT.TB TEST

FDA premarket approval P070006/S016 · decided 2021-03-22

Approval details

PMA number
P070006
Supplement
S016
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
2021-03-09
Decision date
2021-03-22
Days to decision
13 days
Decision code
OK30
Product code
OJN
Advisory committee
Microbiology
Expedited review
No
Location
Milton Park, Abingdon Oxfordshire
Statement
Scale up of batch size for device components.

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