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FRESENIUS COMBILINES LOW VOLUME BLOOD TUBING SET, MODELS 03-2291 (POST PUMP) AND 03-2292 (PRE-PUMP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001107
510(k) Type
Traditional
Applicant
FRESENIUS MEDICAL CARE NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2000
Days to Decision
79 days
Submission Type
Summary

FRESENIUS COMBILINES LOW VOLUME BLOOD TUBING SET, MODELS 03-2291 (POST PUMP) AND 03-2292 (PRE-PUMP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001107
510(k) Type
Traditional
Applicant
FRESENIUS MEDICAL CARE NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2000
Days to Decision
79 days
Submission Type
Summary