Last synced on 25 April 2025 at 11:05 pm

QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030264
510(k) Type
Special
Applicant
JOSTRA AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/26/2003
Days to Decision
30 days
Submission Type
Summary

QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030264
510(k) Type
Special
Applicant
JOSTRA AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/26/2003
Days to Decision
30 days
Submission Type
Summary