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MICROFUSE DUAL RATE INFUSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091386
510(k) Type
Special
Applicant
NUMIA MEDICAL TECHNOLOGY, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2009
Days to Decision
144 days
Submission Type
Summary

MICROFUSE DUAL RATE INFUSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091386
510(k) Type
Special
Applicant
NUMIA MEDICAL TECHNOLOGY, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2009
Days to Decision
144 days
Submission Type
Summary