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LEVITRONIX, THORATEC CENTRIMAG BACK-UP CONSOLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090004
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2009
Days to Decision
13 days
Submission Type
Summary

LEVITRONIX, THORATEC CENTRIMAG BACK-UP CONSOLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090004
510(k) Type
Special
Applicant
LEVITRONIX LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2009
Days to Decision
13 days
Submission Type
Summary