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LEVITRONIX CENTRIMAG EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL L-100

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020271
510(k) Type
Abbreviated
Applicant
Levitronix, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2003
Days to Decision
421 days
Submission Type
Summary

LEVITRONIX CENTRIMAG EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL L-100

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020271
510(k) Type
Abbreviated
Applicant
Levitronix, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2003
Days to Decision
421 days
Submission Type
Summary