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FDA 510(k)

DUCPREP BREAST ASPIRATOR, MODEL PMPO2

K-Number: K993342 · 1999-12-23

ApplicantWindy Hill Technology, Inc.
Decision Date1999-12-23
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DUCPREP BREAST ASPIRATOR, MODEL PMPO2 is the device name listed in this FDA 510(k) record. The listed applicant is Windy Hill Technology, Inc.. It received FDA 510(k) clearance on 1999-12-23 under 510(k) number K993342. 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 DUCPREP BREAST ASPIRATOR, MODEL PMPO2?

DUCPREP BREAST ASPIRATOR, MODEL PMPO2 is a medical device that received FDA 510(k) clearance on 1999-12-23. The listed applicant is Windy Hill Technology, Inc.. The 510(k) number is K993342.

When did DUCPREP BREAST ASPIRATOR, MODEL PMPO2 receive FDA 510(k) clearance?

DUCPREP BREAST ASPIRATOR, MODEL PMPO2 received FDA 510(k) clearance on 1999-12-23, under 510(k) number K993342.

Who is the listed applicant for DUCPREP BREAST ASPIRATOR, MODEL PMPO2?

The FDA 510(k) record lists Windy Hill Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUCPREP BREAST ASPIRATOR, MODEL PMPO2?

The FDA product code for DUCPREP BREAST ASPIRATOR, MODEL PMPO2 is KNW.

Related Clinical Trials

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Other records listing Windy Hill Technology, Inc. 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.

K983867FUJI CATHETER, MODEL CTH001

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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