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LEVITRONIX CENTRIMAG PRIMARY CONSOLE

Page Type
Cleared 510(K)
510(k) Number
K053630
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2006
Days to Decision
28 days
Submission Type
Summary

LEVITRONIX CENTRIMAG PRIMARY CONSOLE

Page Type
Cleared 510(K)
510(k) Number
K053630
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2006
Days to Decision
28 days
Submission Type
Summary