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FDA 510(k)

ADVANTX LCV+

K-Number: K960575 · 1996-05-07

ApplicantGE Medical Systems
Decision Date1996-05-07
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANTX LCV+ 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 1996-05-07 under 510(k) number K960575. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANTX LCV+?

ADVANTX LCV+ is a medical device that received FDA 510(k) clearance on 1996-05-07. The listed applicant is GE Medical Systems. The 510(k) number is K960575.

When did ADVANTX LCV+ receive FDA 510(k) clearance?

ADVANTX LCV+ received FDA 510(k) clearance on 1996-05-07, under 510(k) number K960575.

Who is the listed applicant for ADVANTX LCV+?

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 ADVANTX LCV+?

The FDA product code for ADVANTX LCV+ is IZI.

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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: IZI)

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.

K261037780 nm SPY Portable Handheld Imaging (SPY-PHI) SystemStryker EndoscopyK253181SURGIMAGE SIM 1000H Fluorescence Imaging PlatformSurgimage CorporationK243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbHK243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH

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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