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FDA 510(k)

COOPERSURGICAL TRIAL TRANSFER CATHETER

K-Number: K023384 · 2002-12-13

ApplicantCooper Surgical
Decision Date2002-12-13
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COOPERSURGICAL TRIAL TRANSFER CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Surgical. It received FDA 510(k) clearance on 2002-12-13 under 510(k) number K023384. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOPERSURGICAL TRIAL TRANSFER CATHETER?

COOPERSURGICAL TRIAL TRANSFER CATHETER is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Cooper Surgical. The 510(k) number is K023384.

When did COOPERSURGICAL TRIAL TRANSFER CATHETER receive FDA 510(k) clearance?

COOPERSURGICAL TRIAL TRANSFER CATHETER received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023384.

Who is the listed applicant for COOPERSURGICAL TRIAL TRANSFER CATHETER?

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

What is the FDA product code for COOPERSURGICAL TRIAL TRANSFER CATHETER?

The FDA product code for COOPERSURGICAL TRIAL TRANSFER CATHETER is MQF.

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Other records listing Cooper Surgical 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.

K253698Milex™ Incontinence Dish Pessaries; Milex™ Incontinence Dish Pessaries with Support; Milex™ Cube Pessaries; Milex™ Cube Pessaries with Drainage HolesK091325TEN-YEAR FRACTURE RISK OPTION AND SIRI TABLE OPTION FOR NORLAND DXA BONE DENSITOMETERSK023382COOPERSURGICAL MALLEABLE SYTLETK023383COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETERK023379COOPERSURGICAL EMBRYO TRANSFER CATHETER, COOPERSURGICAL ASSISTED REPRODUCTION CATHETER

Related Devices (Code: MQF)

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.

K253354Minvitro Embryo Transfer Catheters (ETCA23175, ETCA23175-C, ETCB20175, ETCB20175-C, ETCB20175-ET, ETCB20175-ET-C)Guangzhou Hehong Biotech Co., Ltd.K243373Embryo Transfer Catheter (ETC) Assortment: EmbryoCath Embryo Transfer Catheter - Pre-curved 230 mm (REF 17500); EmbryoCath Embryo Transfer Catheter - Straight Malleable 180 mm (REF 17501); EmbryoCath Embryo Transfer Catheter - Straight Malleable 230 mm (REF 17502); EmbryoCath Stylet - 180 mm (REF 17510); EmbryoCath Stylet - 230 mm (REF 17511)Vitrolife Sweden ABK240307VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)Shenzhen Vitavitro Biotech Co., Ltd.K231730FemaSeed Intratubal InseminationFemasys, Inc.K220010Daylily Single Use Sterile Embryo Transfer CatheterShanghai Horizon Medical Technology Co., Ltd.K200248Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft ObturatorsAllwin Medical Devices, 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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