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FDA 510(k)

RI Witness Embryology Heated Plate

K-Number: K160504 · 2016-07-18

ApplicantResearch Instruments Limited
Decision Date2016-07-18
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RI Witness Embryology Heated Plate is the device name listed in this FDA 510(k) record. The listed applicant is Research Instruments Limited. It received FDA 510(k) clearance on 2016-07-18 under 510(k) number K160504. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RI Witness Embryology Heated Plate?

RI Witness Embryology Heated Plate is a medical device that received FDA 510(k) clearance on 2016-07-18. The listed applicant is Research Instruments Limited. The 510(k) number is K160504.

When did RI Witness Embryology Heated Plate receive FDA 510(k) clearance?

RI Witness Embryology Heated Plate received FDA 510(k) clearance on 2016-07-18, under 510(k) number K160504.

Who is the listed applicant for RI Witness Embryology Heated Plate?

The FDA 510(k) record lists Research Instruments Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RI Witness Embryology Heated Plate?

The FDA product code for RI Witness Embryology Heated Plate is MQG.

Other records listing Research Instruments Limited as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MQG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260194Vacuum Pump (Model: AD-VPUM-500)Sheng Sheng Yi (Beijing) Technology Company LimitedK242684Harioculture TL-16 Time-lapse IncubatorHua Yue Medical Technology Co., Ltd.K232493Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)Wuhan Huchuang Union Technology Co., Ltd.K180188Geri Embryo Incubator with Geri Connect and Geri Assess Software, and Geri DishGenea Biomedx Pty, Ltd.K173264EmbryoScope+Vitrolife A/SK180304Geri Embryo Incubator and Geri DishGenea Biomedx Pty, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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