Atlas FDA

BRAHMS DIAGNOSTICA DYNOTEST TG-PLUS

FDA 510(k) clearance K021057 · decided 2002-09-17

Clearance details

K-number
K021057
Device name
BRAHMS DIAGNOSTICA DYNOTEST TG-PLUS
Applicant
Brahms Diagnostica, LLC
Decision
Substantially Equivalent
Date received
2002-04-01
Decision date
2002-09-17
Days to decision
169 days
Clearance type
Traditional
Product code
MSW
Device class
2
Regulation number
866.6010
Medical specialty
Immunology
Advisory committee
Immunology
Location
Norcross, GA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.