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FDA 510(k)

BMN I TYPE MARROW ASPIRATION NEEDLE

K-Number: K020987 · 2002-06-25

ApplicantH.S. Hospital Service S.R.L.
Decision Date2002-06-25
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BMN I TYPE MARROW ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is H.S. Hospital Service S.R.L.. It received FDA 510(k) clearance on 2002-06-25 under 510(k) number K020987. 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 BMN I TYPE MARROW ASPIRATION NEEDLE?

BMN I TYPE MARROW ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 2002-06-25. The listed applicant is H.S. Hospital Service S.R.L.. The 510(k) number is K020987.

When did BMN I TYPE MARROW ASPIRATION NEEDLE receive FDA 510(k) clearance?

BMN I TYPE MARROW ASPIRATION NEEDLE received FDA 510(k) clearance on 2002-06-25, under 510(k) number K020987.

Who is the listed applicant for BMN I TYPE MARROW ASPIRATION NEEDLE?

The FDA 510(k) record lists H.S. Hospital Service S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BMN I TYPE MARROW ASPIRATION NEEDLE?

The FDA product code for BMN I TYPE MARROW ASPIRATION NEEDLE is KNW.

Related Clinical Trials

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Other records listing H.S. Hospital Service S.R.L. 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.

K021525TOPCUTK013692TRAPSYSTEM SETK002947BIOMOL ASPIRATION BIOPSY NEEDLEK002944PRECISA BIOPSY NEEDLEK002946SILENT BIOPSY NEEDLE

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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