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FDA 510(k)

PROMOTOR FINAL RINSE SPERM WASH MEDIUM

K-Number: K024290 · 2003-03-03

ApplicantCeres Fertility, Inc.
Decision Date2003-03-03
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PROMOTOR FINAL RINSE SPERM WASH MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Ceres Fertility, Inc.. It received FDA 510(k) clearance on 2003-03-03 under 510(k) number K024290. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROMOTOR FINAL RINSE SPERM WASH MEDIUM?

PROMOTOR FINAL RINSE SPERM WASH MEDIUM is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Ceres Fertility, Inc.. The 510(k) number is K024290.

When did PROMOTOR FINAL RINSE SPERM WASH MEDIUM receive FDA 510(k) clearance?

PROMOTOR FINAL RINSE SPERM WASH MEDIUM received FDA 510(k) clearance on 2003-03-03, under 510(k) number K024290.

Who is the listed applicant for PROMOTOR FINAL RINSE SPERM WASH MEDIUM?

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

What is the FDA product code for PROMOTOR FINAL RINSE SPERM WASH MEDIUM?

The FDA product code for PROMOTOR FINAL RINSE SPERM WASH MEDIUM is MQL.

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 Ceres Fertility, 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.

K023106PROMOTOR

Related Devices (Code: MQL)

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.

K254261Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.K260248Ultra-Fast WarmKitazato CorporationK252672CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)Casebioscience, Inc.K250445Fast Warm - NXFujifilm Irvine ScientificK251637Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle Flushing Solution, Dewin One Step medium [with HSA and without HSA])Donnevie Medical Technology (Shanghai) Co. , Ltd.K251305Ultra-Fast Vitri; Ultra-Fast WarmKitazato Corporation

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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