Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201

K-Number: K000950 · 2000-05-12

ApplicantLabotect Labor-Technik Gottingen
Decision Date2000-05-12
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201 is the device name listed in this FDA 510(k) record. The listed applicant is Labotect Labor-Technik Gottingen. It received FDA 510(k) clearance on 2000-05-12 under 510(k) number K000950. 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 EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201?

EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201 is a medical device that received FDA 510(k) clearance on 2000-05-12. The listed applicant is Labotect Labor-Technik Gottingen. The 510(k) number is K000950.

When did EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201 receive FDA 510(k) clearance?

EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201 received FDA 510(k) clearance on 2000-05-12, under 510(k) number K000950.

Who is the listed applicant for EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201?

The FDA 510(k) record lists Labotect Labor-Technik Gottingen as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201?

The FDA product code for EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201 is MQF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Labotect Labor-Technik Gottingen 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.

K021438INSEMINATION CATHETER, MODEL 320301K003056OVARIAL BIOPSY SET 324102-324108; OVARIAL BIOPSY SET 324200-324202; OVARIAL BIOPSY NEEDLE 32218

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

View on FDA Database →

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

↑