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FDA 510(k)

G-MOPS G5 SERIES

K-Number: K081115 · 2008-09-17

ApplicantVitrolife Sweden AB
Decision Date2008-09-17
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

G-MOPS G5 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Vitrolife Sweden AB. It received FDA 510(k) clearance on 2008-09-17 under 510(k) number K081115. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-MOPS G5 SERIES?

G-MOPS G5 SERIES is a medical device that received FDA 510(k) clearance on 2008-09-17. The listed applicant is Vitrolife Sweden AB. The 510(k) number is K081115.

When did G-MOPS G5 SERIES receive FDA 510(k) clearance?

G-MOPS G5 SERIES received FDA 510(k) clearance on 2008-09-17, under 510(k) number K081115.

Who is the listed applicant for G-MOPS G5 SERIES?

The FDA 510(k) record lists Vitrolife Sweden AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G-MOPS G5 SERIES?

The FDA product code for G-MOPS G5 SERIES is MQL.

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Related Devices (Code: MQL)

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.

K254261Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.K260248Ultra-Fast WarmKitazato CorporationK252672CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)Casebioscience, Inc.K250445Fast Warm - NXFujifilm Irvine ScientificK251637Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle Flushing Solution, Dewin One Step medium [with HSA and without HSA])Donnevie Medical Technology (Shanghai) Co. , Ltd.K251305Ultra-Fast Vitri; Ultra-Fast WarmKitazato Corporation

Official Source

View on FDA Database →

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

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