510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MQJClass II

Micromanipulators And Microinjectors, Assisted Reproduction

21 CFR 884.6150 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

MQJ is the FDA product code for Micromanipulators And Microinjectors, Assisted Reproduction, a class II device type, regulated under 21 CFR 884.6150. As of , FDA records hold 23 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MQJ
Device name
Micromanipulators And Microinjectors, Assisted Reproduction
Regulation
21 CFR 884.6150
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
23
Ingested recalls
1

Clearances, product code MQJ

By decision year
23 clearances under product code MQJ with a decision year between 2000 and 2015, 2000 the highest year at 18.
Show the numbers
510(k) clearances under FDA product code MQJ by decision year
YearClearances
200018
20012
20122
20151

Applicants with the most clearances

Product code MQJ
Applicants holding the most 510(k) clearances under product code MQJ
ApplicantClearances
Narishige Co., Ltd.20
<Genx> Intl., Inc.1
Eppendorf AG1
Research Instruments Ltd1

Companies listing this code with FDA

Companies whose registered establishments list this code