EMBRYON ULTRASOUND NEEDLE GUIDE— 510(k) K032015

Substantially Equivalent

Rocket Medical Plc

FDA 510(k) clearance K032015 for EMBRYON ULTRASOUND NEEDLE GUIDE, Substantially Equivalent on 2003-08-08. Applicant: Rocket Medical Plc. Device class: 2.

Clearance details

Applicant
Rocket Medical Plc
Product code
Code MQE
Device class
Class 2
Regulation
21 CFR 884.6100
Advisory panel
Obstetrics/Gynecology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, Tyne & Wear, GB
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