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FDA 510(k)

OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH

K-Number: K051742 · 2005-10-07

ApplicantInntec, Inc.
Decision Date2005-10-07
Product CodeMQE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH is the device name listed in this FDA 510(k) record. The listed applicant is Inntec, Inc.. It received FDA 510(k) clearance on 2005-10-07 under 510(k) number K051742. 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 OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH?

OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Inntec, Inc.. The 510(k) number is K051742.

When did OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH receive FDA 510(k) clearance?

OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH received FDA 510(k) clearance on 2005-10-07, under 510(k) number K051742.

Who is the listed applicant for OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH?

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

What is the FDA product code for OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH?

The FDA product code for OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH is MQE.

Related Clinical Trials

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Other records listing Inntec, 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.

K052059IUI CATHETER, MODEL 9057K050521EMBRYO TRANSFER CATHETER WITH ACCESSORY STYLET, MODELS 9018, 9023, 9018-S, 9023-S

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

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

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