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FDA 510(k)

WISCONSIN DUAL-PHOTON BONE ANALYZER

K-Number: K802180 · 1980-12-31

ApplicantLunar Radiation Corp.
Decision Date1980-12-31
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WISCONSIN DUAL-PHOTON BONE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Lunar Radiation Corp.. It received FDA 510(k) clearance on 1980-12-31 under 510(k) number K802180. 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 WISCONSIN DUAL-PHOTON BONE ANALYZER?

WISCONSIN DUAL-PHOTON BONE ANALYZER is a medical device that received FDA 510(k) clearance on 1980-12-31. The listed applicant is Lunar Radiation Corp.. The 510(k) number is K802180.

When did WISCONSIN DUAL-PHOTON BONE ANALYZER receive FDA 510(k) clearance?

WISCONSIN DUAL-PHOTON BONE ANALYZER received FDA 510(k) clearance on 1980-12-31, under 510(k) number K802180.

Who is the listed applicant for WISCONSIN DUAL-PHOTON BONE ANALYZER?

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

What is the FDA product code for WISCONSIN DUAL-PHOTON BONE ANALYZER?

The FDA product code for WISCONSIN DUAL-PHOTON BONE ANALYZER is KGI.

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 Lunar Radiation 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.

K873296DPX BONE DENSITOMETERK810159BONE MINERAL ANALYZER CONTROLLERK810140DUAL-PHOTON TOTAL BODY BONE MINERAL ANAK802181WISCONSIN BONE MINERAL ANALYZERK802182WISCONSIN HEART RATE MONITOR

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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