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DIALGUARD ENDOTOXIN REMOVAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993806
510(k) Type
Traditional
Applicant
CLARIGEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2000
Days to Decision
279 days
Submission Type
Summary

DIALGUARD ENDOTOXIN REMOVAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993806
510(k) Type
Traditional
Applicant
CLARIGEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2000
Days to Decision
279 days
Submission Type
Summary