<GEN>SINGLE LUMEN NEEDLE— 510(k) K991262

Substantially Equivalent

<Genx> Intl., Inc.

FDA 510(k) clearance K991262 for <GEN>SINGLE LUMEN NEEDLE, Substantially Equivalent on 1999-09-09. Applicant: <Genx> Intl., Inc..

Clearance details

Applicant: <Genx> Intl., Inc.
Product code: Code MQE
Advisory panel: Obstetrics/Gynecology
Date received: 1999-04-13
Decision date: 1999-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, CT, US

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