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FDA 510(k)

GRICE SOFT TISSUE BIOPSY KIT

K-Number: K922161 · 1992-10-13

ApplicantIdeal Medical, Inc.
Decision Date1992-10-13
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GRICE SOFT TISSUE BIOPSY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ideal Medical, Inc.. It received FDA 510(k) clearance on 1992-10-13 under 510(k) number K922161. 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 GRICE SOFT TISSUE BIOPSY KIT?

GRICE SOFT TISSUE BIOPSY KIT is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K922161.

When did GRICE SOFT TISSUE BIOPSY KIT receive FDA 510(k) clearance?

GRICE SOFT TISSUE BIOPSY KIT received FDA 510(k) clearance on 1992-10-13, under 510(k) number K922161.

Who is the listed applicant for GRICE SOFT TISSUE BIOPSY KIT?

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

What is the FDA product code for GRICE SOFT TISSUE BIOPSY KIT?

The FDA product code for GRICE SOFT TISSUE BIOPSY KIT is KNW.

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Other records listing Ideal Medical, 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.

K944067PEANUT WAND, MODIFICATIONK931115HATCHER STONE-EMBOLIS EXTRACTORK926335IDEAS PEANUT WANDK921922GRICE LAPAROSCOPIC SUTURING NEEDLEK915175REDDICK RETRACTORK914880DUAL BALLOON EMBOLECTOMY CATHETER

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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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