Atlas FDA

C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE TEST SYSTEM FOR COBAS INTEGRA INSTRUMENTS

FDA 510(k) clearance K053603 · decided 2006-02-09

Clearance details

K-number
K053603
Device name
C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE TEST SYSTEM FOR COBAS INTEGRA INSTRUMENTS
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2005-12-23
Decision date
2006-02-09
Days to decision
48 days
Clearance type
Traditional
Product code
NQD
Device class
2
Regulation number
866.5270
Medical specialty
Immunology
Advisory committee
Immunology
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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