Atlas FDA

ACCU-CHEK ADVANTAGE METER

FDA 510(k) clearance K000365 · decided 2000-02-23

Clearance details

K-number
K000365
Device name
ACCU-CHEK ADVANTAGE METER
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2000-02-04
Decision date
2000-02-23
Days to decision
19 days
Clearance type
Special
Product code
CGA
Device class
2
Regulation number
862.1345
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
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.

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