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)

UC-CARE WARMING SYSTEM

K-Number: K090978 · 2009-08-10

ApplicantUC-CARE , Ltd.
Decision Date2009-08-10
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UC-CARE WARMING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is UC-CARE , Ltd.. It received FDA 510(k) clearance on 2009-08-10 under 510(k) number K090978. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UC-CARE WARMING SYSTEM?

UC-CARE WARMING SYSTEM is a medical device that received FDA 510(k) clearance on 2009-08-10. The listed applicant is UC-CARE , Ltd.. The 510(k) number is K090978.

When did UC-CARE WARMING SYSTEM receive FDA 510(k) clearance?

UC-CARE WARMING SYSTEM received FDA 510(k) clearance on 2009-08-10, under 510(k) number K090978.

Who is the listed applicant for UC-CARE WARMING SYSTEM?

The FDA 510(k) record lists UC-CARE , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UC-CARE WARMING SYSTEM?

The FDA product code for UC-CARE WARMING SYSTEM is GEH.

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 UC-CARE , Ltd. 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.

K260161SmartGuide Disposable Guides and GridsK250664Navigo Workstation 2.3 (FPRMC00039)K173054Navigo Workstation Version 2.0K160934UC-CARE NaviGo WorkstationK100784UC-CARE NAVIGO SYTEM

Related Devices (Code: GEH)

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.

K262420Maverix Cryo Biopsy Pro (MCB Pro) (MCBP-1000); Maverix Cryo Cartridge (CC-1000)Serpex MedicalK261068Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)Serpex MedicalK261806ERBECRYO 2 Cryosurgical Unit and AccessoriesErbe Elektromedizin GmbHK253230ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit; Erbe Flexible CryoprobeErbe Elektromedizin GmbHK252198Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover)Medical Brands Laboratories B.V.K260377XSense Cryoablation System with CryoProbesIceCure Medical , Ltd.

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.

↑