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FDA 510(k)

MANAN MENGHINI NEEDLE

K-Number: K851836 · 1985-06-21

ApplicantManan Manufacturing Co., Inc.
Decision Date1985-06-21
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MANAN MENGHINI NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Manan Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1985-06-21 under 510(k) number K851836. 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 MANAN MENGHINI NEEDLE?

MANAN MENGHINI NEEDLE is a medical device that received FDA 510(k) clearance on 1985-06-21. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K851836.

When did MANAN MENGHINI NEEDLE receive FDA 510(k) clearance?

MANAN MENGHINI NEEDLE received FDA 510(k) clearance on 1985-06-21, under 510(k) number K851836.

Who is the listed applicant for MANAN MENGHINI NEEDLE?

The FDA 510(k) record lists Manan Manufacturing Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MANAN MENGHINI NEEDLE?

The FDA product code for MANAN MENGHINI NEEDLE is KNW.

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Other records listing Manan Manufacturing Co., 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.

K873208MANAN TURNER STYLE NEEDLEK864405MANAN CONTRAST MEDIA ADMINISTRATION SETK863848MANAN BREST TUMOR LOCALIZATION NEEDLEK852018ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHRK852501MYELOGRAM PROCEDURE TRAYK851832NAMAN POTTS COURNAND NEEDLE

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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