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FDA 510(k)

LILY MULTICANNULA GUIDE

K-Number: K954999 · 1996-04-04

ApplicantLily Imaging Solutions Co.
Decision Date1996-04-04
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LILY MULTICANNULA GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Lily Imaging Solutions Co.. It received FDA 510(k) clearance on 1996-04-04 under 510(k) number K954999. 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 LILY MULTICANNULA GUIDE?

LILY MULTICANNULA GUIDE is a medical device that received FDA 510(k) clearance on 1996-04-04. The listed applicant is Lily Imaging Solutions Co.. The 510(k) number is K954999.

When did LILY MULTICANNULA GUIDE receive FDA 510(k) clearance?

LILY MULTICANNULA GUIDE received FDA 510(k) clearance on 1996-04-04, under 510(k) number K954999.

Who is the listed applicant for LILY MULTICANNULA GUIDE?

The FDA 510(k) record lists Lily Imaging Solutions Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LILY MULTICANNULA GUIDE?

The FDA product code for LILY MULTICANNULA GUIDE 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.

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Other records listing Lily Imaging Solutions Co. 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.

K954998LILY DARK VIEWER

Related Devices (Code: KNW)

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.

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, LLCK261196Promisemed 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

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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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