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<GEN>SINGLE LUMEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K991262
510(k) Type
Traditional
Applicant
<GENX> INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1999
Days to Decision
149 days
Submission Type
Summary

<GEN>SINGLE LUMEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K991262
510(k) Type
Traditional
Applicant
<GENX> INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1999
Days to Decision
149 days
Submission Type
Summary