FDA 510(k)

MD TECH BIOPSY SET FOR BONE AND BONE MARROW

K-Number: K980196 · 1998-02-03

ApplicantMedical Device Technologies, Inc.

Decision Date1998-02-03

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MD TECH BIOPSY SET FOR BONE AND BONE MARROW is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 1998-02-03 under 510(k) number K980196. 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 MD TECH BIOPSY SET FOR BONE AND BONE MARROW?

MD TECH BIOPSY SET FOR BONE AND BONE MARROW is a medical device that received FDA 510(k) clearance on 1998-02-03. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K980196.

When did MD TECH BIOPSY SET FOR BONE AND BONE MARROW receive FDA 510(k) clearance?

MD TECH BIOPSY SET FOR BONE AND BONE MARROW received FDA 510(k) clearance on 1998-02-03, under 510(k) number K980196.

Who is the listed applicant for MD TECH BIOPSY SET FOR BONE AND BONE MARROW?

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

What is the FDA product code for MD TECH BIOPSY SET FOR BONE AND BONE MARROW?

The FDA product code for MD TECH BIOPSY SET FOR BONE AND BONE MARROW 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

Other records listing Medical Device Technologies, Inc. as applicant

K101832BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT K053518INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR K051421INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR K050873CANALIZER HYDROPHILIC GUIDE WIRE K043523INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE K042464V-CORE FULL CORE BREAST BIOPSY INSTRUMENT

View all 46 devices →

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.