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FDA 510(k)

HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT

K-Number: K881957 · 1988-05-20

ApplicantN-S Medical Products
Decision Date1988-05-20
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT is the device name listed in this FDA 510(k) record. The listed applicant is N-S Medical Products. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K881957. 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 HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT?

HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is N-S Medical Products. The 510(k) number is K881957.

When did HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT receive FDA 510(k) clearance?

HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT received FDA 510(k) clearance on 1988-05-20, under 510(k) number K881957.

Who is the listed applicant for HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT?

The FDA 510(k) record lists N-S Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT?

The FDA product code for HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT 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 N-S Medical Products 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.

K880287TRU-TRAC COILED GUIDEWIREK880288TRU-TRAC TORQUE GUIDEWIREK881956NATIONAL-STANDARD NEEDLE HOLDERK870523HAWKINS BREAST LOCALIZATION 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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