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FDA 510(k)

ADMS SILENT NEEDLE GUN

K-Number: K882746 · 1989-03-17

ApplicantAdvanced Diagnostic Medical Systems, Inc.
Decision Date1989-03-17
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADMS SILENT NEEDLE GUN is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. It received FDA 510(k) clearance on 1989-03-17 under 510(k) number K882746. 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 ADMS SILENT NEEDLE GUN?

ADMS SILENT NEEDLE GUN is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. The 510(k) number is K882746.

When did ADMS SILENT NEEDLE GUN receive FDA 510(k) clearance?

ADMS SILENT NEEDLE GUN received FDA 510(k) clearance on 1989-03-17, under 510(k) number K882746.

Who is the listed applicant for ADMS SILENT NEEDLE GUN?

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

What is the FDA product code for ADMS SILENT NEEDLE GUN?

The FDA product code for ADMS SILENT NEEDLE GUN 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 Advanced Diagnostic Medical Systems, 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.

K890203ADMS BIOPSY NEEDLEK881208PROBE SHEATH FOR ADMS ULTRASOUND PROBEK875119BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE

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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