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FDA 510(k)

LIFE IMAGING SYSTEMS LIS 6000 A

K-Number: K961403 · 1996-07-03

ApplicantLife Imaging Systems, Inc.
Decision Date1996-07-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIFE IMAGING SYSTEMS LIS 6000 A is the device name listed in this FDA 510(k) record. The listed applicant is Life Imaging Systems, Inc.. It received FDA 510(k) clearance on 1996-07-03 under 510(k) number K961403. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE IMAGING SYSTEMS LIS 6000 A?

LIFE IMAGING SYSTEMS LIS 6000 A is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Life Imaging Systems, Inc.. The 510(k) number is K961403.

When did LIFE IMAGING SYSTEMS LIS 6000 A receive FDA 510(k) clearance?

LIFE IMAGING SYSTEMS LIS 6000 A received FDA 510(k) clearance on 1996-07-03, under 510(k) number K961403.

Who is the listed applicant for LIFE IMAGING SYSTEMS LIS 6000 A?

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

What is the FDA product code for LIFE IMAGING SYSTEMS LIS 6000 A?

The FDA product code for LIFE IMAGING SYSTEMS LIS 6000 A is LLZ.

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 Life Imaging 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.

K990560LIFE IMAGING SYSTEMS, MODEL L3DI

Related Devices (Code: LLZ)

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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