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FDA 510(k)

PRODIGY LATERAL VIEW SOFTWARE

K-Number: K000826 · 2000-04-14

ApplicantLunar Corp.
Decision Date2000-04-14
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRODIGY LATERAL VIEW SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Lunar Corp.. It received FDA 510(k) clearance on 2000-04-14 under 510(k) number K000826. The device is classified under product code KGI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRODIGY LATERAL VIEW SOFTWARE?

PRODIGY LATERAL VIEW SOFTWARE is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Lunar Corp.. The 510(k) number is K000826.

When did PRODIGY LATERAL VIEW SOFTWARE receive FDA 510(k) clearance?

PRODIGY LATERAL VIEW SOFTWARE received FDA 510(k) clearance on 2000-04-14, under 510(k) number K000826.

Who is the listed applicant for PRODIGY LATERAL VIEW SOFTWARE?

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

What is the FDA product code for PRODIGY LATERAL VIEW SOFTWARE?

The FDA product code for PRODIGY LATERAL VIEW SOFTWARE is KGI.

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Other records listing Lunar Corp. 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.

K001812PEDIATRIC REFERENCE DATAK001756LUNAR REPORT GENERATOR IIK983564PRODIGY TOTAL BODY SOFTWAREK983724ORCA-DX BONE DENSITOMETERK983269FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETERK983262FRACTURE RISK ASSESSMENT OPTION FOR PIXI BONE DENSITOMETERS

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Related Devices (Code: KGI)

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.

K254072BoneVueCurvebeam AI / Curvebeam, LLCK252718Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLCK2510223D-SHAPER3D-Shaper Medical S.LK242295BunkerHill BMDBunkerHill HealthK243218TBS iNsight (V4)Medimaps Group SAK220402VirtuOstO.N. Diagnostics

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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