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LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES

Page Type
Cleared 510(K)
510(k) Number
K093832
510(k) Type
Special
Applicant
Levitronix, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2010
Days to Decision
30 days
Submission Type
Summary

LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES

Page Type
Cleared 510(K)
510(k) Number
K093832
510(k) Type
Special
Applicant
Levitronix, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2010
Days to Decision
30 days
Submission Type
Summary