FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WORKBENCH BY <GENX>

K Number: K020560 · Decision Jun 19, 2002
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
45
Applicant Total
8
Review Days
119

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Basic Information

Device Name
WORKBENCH BY <GENX>
K Number
K020560
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6120
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Genx Intl., Inc.
Date Received
February 20, 2002
Decision Date
June 19, 2002
Product Code
MQG
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQG Accessory, Assisted Reproduction

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K092578 LIFEGLOBAL PROTEIN SUPPLEMENT
K083509 LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA
K070689 LG SPERM FREEZING
K962816 SPERM PREPARATION MEDIA
K963031 GENXCATHETER