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<GENX> DOUBLE LUMEN NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991020
510(k) Type
Traditional
Applicant
<GENX> INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1999
Days to Decision
164 days
Submission Type
Summary

<GENX> DOUBLE LUMEN NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991020
510(k) Type
Traditional
Applicant
<GENX> INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1999
Days to Decision
164 days
Submission Type
Summary