Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

G-2 V5

K-Number: K081117 · 2008-09-16

Decision Date2008-09-16
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

G-2 V5 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 2008-09-16 under 510(k) number K081117. 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-2 V5?

G-2 V5 is a medical device that received FDA 510(k) clearance on 2008-09-16. The listed applicant is Vitrolife Sweden AB. The 510(k) number is K081117.

When did G-2 V5 receive FDA 510(k) clearance?

G-2 V5 received FDA 510(k) clearance on 2008-09-16, under 510(k) number K081117.

Who is the listed applicant for G-2 V5?

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-2 V5?

The FDA product code for G-2 V5 is MQL.

Other records listing Vitrolife Sweden AB 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.

View all 36 devices →

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.

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.

↑