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FDA 510(k)

LIFE IMAGING SYSTEMS, MODEL L3DI

K-Number: K990560 · 1999-05-20

ApplicantLife Imaging Systems, Inc.
Decision Date1999-05-20
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIFE IMAGING SYSTEMS, MODEL L3DI 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 1999-05-20 under 510(k) number K990560. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE IMAGING SYSTEMS, MODEL L3DI?

LIFE IMAGING SYSTEMS, MODEL L3DI is a medical device that received FDA 510(k) clearance on 1999-05-20. The listed applicant is Life Imaging Systems, Inc.. The 510(k) number is K990560.

When did LIFE IMAGING SYSTEMS, MODEL L3DI receive FDA 510(k) clearance?

LIFE IMAGING SYSTEMS, MODEL L3DI received FDA 510(k) clearance on 1999-05-20, under 510(k) number K990560.

Who is the listed applicant for LIFE IMAGING SYSTEMS, MODEL L3DI?

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, MODEL L3DI?

The FDA product code for LIFE IMAGING SYSTEMS, MODEL L3DI is IYO.

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.

K961403LIFE IMAGING SYSTEMS LIS 6000 A

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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