FDA 510(k)

WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS

K-Number: K031622 · 2003-06-26

Decision Date2003-06-26

Product CodeMQE

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS is the device name listed in this FDA 510(k) record. The listed applicant is Portex , Ltd.. It received FDA 510(k) clearance on 2003-06-26 under 510(k) number K031622. The device is classified under product code MQE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS?

WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS is a medical device that received FDA 510(k) clearance on 2003-06-26. The listed applicant is Portex , Ltd.. The 510(k) number is K031622.

When did WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS receive FDA 510(k) clearance?

WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS received FDA 510(k) clearance on 2003-06-26, under 510(k) number K031622.

Who is the listed applicant for WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS?

The FDA 510(k) record lists Portex , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS?

The FDA product code for WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS is MQE.

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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.