FDA 510(k)

SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER

K-Number: K884900 · 1989-01-13

ApplicantSiemens Medical Solutions USA, Inc.

Decision Date1989-01-13

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1989-01-13 under 510(k) number K884900. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER?

SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER is a medical device that received FDA 510(k) clearance on 1989-01-13. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K884900.

When did SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER receive FDA 510(k) clearance?

SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER received FDA 510(k) clearance on 1989-01-13, under 510(k) number K884900.

Who is the listed applicant for SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER?

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

What is the FDA product code for SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER?

The FDA product code for SIEMENS SECTOR 3.5 AND 5.0 MHZ CDA TRANSDUCER is KNW.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: KNW)

K260517Automatic Core Biopsy InstrumentZhejiang Curaway Medical Technology Co., Ltd.K262571EnCor EnCompass™ Breast Biopsy and Tissue Removal SystemBard Peripheral Vascular, Inc.K262792Brevera Biopsy System with CorLumina Imaging Technology (BREVDISP09)Hologic, Inc.K260572Marrow MarxmanMedimetrix, LLC K261196Promisemed VeriEcto Automatic Biopsy NeedlesPromisemed Hangzhou Meditech Co., Ltd.K260365Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Control Module; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Probe, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Targeting Set, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Foot Switch; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Reusable Tray; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Battery CharDevicor Medical Products, 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.