Atlas FDA

CONTROL SET DAT I, CONTRL SET DAT II, CONTROL SET DAT III, CONTROL SET AMPHETAMINE 1000 AND CONTROL SET AMPHETAMINE 500

FDA 510(k) clearance K080183 · decided 2008-03-25

Clearance details

K-number
K080183
Device name
CONTROL SET DAT I, CONTRL SET DAT II, CONTROL SET DAT III, CONTROL SET AMPHETAMINE 1000 AND CONTROL SET AMPHETAMINE 500
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2008-01-25
Decision date
2008-03-25
Days to decision
60 days
Clearance type
Abbreviated
Product code
DIF
Device class
1
Regulation number
862.3280
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

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