Last synced on 9 May 2025 at 11:05 pm

ELITE-I (BI) DUAL LUMEN CATHETER; ELITE-I (RA) DUAL LUMEN CATHETER; ELITE-I (BIX)DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130639
510(k) Type
Special
Applicant
MAQUET CARDIOPULMONARY AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/16/2013
Days to Decision
66 days
Submission Type
Summary

ELITE-I (BI) DUAL LUMEN CATHETER; ELITE-I (RA) DUAL LUMEN CATHETER; ELITE-I (BIX)DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130639
510(k) Type
Special
Applicant
MAQUET CARDIOPULMONARY AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/16/2013
Days to Decision
66 days
Submission Type
Summary