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FDA 510(k)

MONA LISA ASPIRATION NEEDLE

K-Number: K032208 · 2003-12-09

ApplicantFertility Technology Resources, Inc.
Decision Date2003-12-09
Product CodeMQE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MONA LISA ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Fertility Technology Resources, Inc.. It received FDA 510(k) clearance on 2003-12-09 under 510(k) number K032208. 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 MONA LISA ASPIRATION NEEDLE?

MONA LISA ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 2003-12-09. The listed applicant is Fertility Technology Resources, Inc.. The 510(k) number is K032208.

When did MONA LISA ASPIRATION NEEDLE receive FDA 510(k) clearance?

MONA LISA ASPIRATION NEEDLE received FDA 510(k) clearance on 2003-12-09, under 510(k) number K032208.

Who is the listed applicant for MONA LISA ASPIRATION NEEDLE?

The FDA 510(k) record lists Fertility Technology Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONA LISA ASPIRATION NEEDLE?

The FDA product code for MONA LISA ASPIRATION NEEDLE is MQE.

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Other records listing Fertility Technology Resources, Inc. 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.

K041470MORTON IUI CATHETERSK023017TUCKER EMBRYO CATHETERK992307EMBRYO GLIDE EMBRYO TRANSFER CATHETER, EMBRYO GLIDE STYLE FOR EMBRYO TRANSFER CATHETER

Related Devices (Code: MQE)

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.

K253121Giftlife Single Lumen Oocyte Retrieval Needle, Giftlife Double Lumen Oocyte Retrieval NeedleGimbo Medical Technology Shenzhen Co., Ltd.K240523VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G)Shenzhen Vitavitro Biotech Co., Ltd.K232163Lotus Single Lumen Ovum Aspiration Needle; Lotus Double Lumen Ovum Aspiration NeedleZhejiang Horizon Medical Technology Co., Ltd.K190590Allwin Ovum Pickup Needles (ACE Single Lumen Ovum Pickup Needle, OVUMPICK Double Lumen Ovum Pickup Needle, ACE-FL Single Lumen Ovum Pickup Needle with Flushing Line, ACE-M Manual Single Lumen Ovum Pickup Needle)Allwin Medical Devices, Inc.K191291Wallace Dual Lumen Oocyte Recovery SystemCooperSurgical, Inc.K182959Wallace Dual Lumen Oocyte Recovery SystemCooperSurgical, Inc.

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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