Last synced on 14 November 2025 at 11:06 pm

LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITOR

Page Type
Cleared 510(K)
510(k) Number
K102129
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
29 days
Submission Type
Summary

LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITOR

Page Type
Cleared 510(K)
510(k) Number
K102129
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
29 days
Submission Type
Summary