Atlas FDA

COBAS LITHIUM

FDA 510(k) clearance K063684 · decided 2008-03-21

Clearance details

K-number
K063684
Device name
COBAS LITHIUM
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2006-12-12
Decision date
2008-03-21
Days to decision
465 days
Clearance type
Traditional
Product code
NDW
Device class
2
Regulation number
862.3560
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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