Last synced on 14 November 2025 at 11:06 pm

LEVITRONIX CENTRIMAG BACK-UP CONSOLE

Page Type
Cleared 510(K)
510(k) Number
K051209
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2005
Days to Decision
120 days
Submission Type
Summary

LEVITRONIX CENTRIMAG BACK-UP CONSOLE

Page Type
Cleared 510(K)
510(k) Number
K051209
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2005
Days to Decision
120 days
Submission Type
Summary