Atlas FDA

SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 2, MODEL A8096

FDA 510(k) clearance K013544 · decided 2001-11-15

Clearance details

K-number
K013544
Device name
SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 2, MODEL A8096
Applicant
Sigma Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
2001-10-24
Decision date
2001-11-15
Days to decision
22 days
Clearance type
Traditional
Product code
DAP
Device class
2
Regulation number
864.7320
Medical specialty
Hematology
Advisory committee
Hematology
Location
St. Louis, MO, US
Third-party review
No
Expedited review
No

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STRATUS CS ACUTE CARE D-DIMER (K110303)Siemens Healthcare Diagnostics2011-05-16
INNOVANCE D-DIMER, MODEL OPBP09 (K093626)Siemens Healthcare Diagnostics2010-11-29
HEMOSIL D-DIMER HS 500, CONTROLS (K090264)Instrumentation Laboratory CO2010-02-05
INNOVANCE D-DIMER, MODEL OPBP09 (K091916)Siemens Healthcare Diagnostics2009-10-29
INNOVANCE D-DIMER AND INNOVANCE D-DIMER CONTROLS (K081732)Siemens Healthcare Diagnostics2008-10-24
HEMOSIL D-DIMER (K073042)Instrumentation Laboratory2008-07-31

Recalls involving this device

No recalls on record reference this clearance.