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FDA 510(k)

G-PGD

K-Number: K033101 · 2004-05-07

ApplicantVitrolife Sweden AB
Decision Date2004-05-07
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

G-PGD 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 2004-05-07 under 510(k) number K033101. 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-PGD?

G-PGD is a medical device that received FDA 510(k) clearance on 2004-05-07. The listed applicant is Vitrolife Sweden AB. The 510(k) number is K033101.

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

G-PGD received FDA 510(k) clearance on 2004-05-07, under 510(k) number K033101.

Who is the listed applicant for G-PGD?

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-PGD?

The FDA product code for G-PGD is MQL.

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Related Devices (Code: MQL)

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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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