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FDA 510(k)

GE LOGIQ 700

K-Number: K001016 · 2000-04-24

ApplicantGE Medical Systems
Decision Date2000-04-24
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 700 is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 2000-04-24 under 510(k) number K001016. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE LOGIQ 700?

GE LOGIQ 700 is a medical device that received FDA 510(k) clearance on 2000-04-24. The listed applicant is GE Medical Systems. The 510(k) number is K001016.

When did GE LOGIQ 700 receive FDA 510(k) clearance?

GE LOGIQ 700 received FDA 510(k) clearance on 2000-04-24, under 510(k) number K001016.

Who is the listed applicant for GE LOGIQ 700?

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

What is the FDA product code for GE LOGIQ 700?

The FDA product code for GE LOGIQ 700 is ITX.

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Other records listing GE Medical Systems 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.

K253808AIR Recon DLK220848Venue FitK220851VenueK173341Vivid E80, Vivid E90, Vivid E95K103411IDEAL IQ SOFTWARE OPTIONK073138CARDIQ EXPRESS VERSION 2.0

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Related Devices (Code: ITX)

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.

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, 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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