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FDA 510(k)

DUAL-PHOTON TOTAL BODY BONE MINERAL ANA

K-Number: K810140 · 1981-02-12

ApplicantLunar Radiation Corp.
Decision Date1981-02-12
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DUAL-PHOTON TOTAL BODY BONE MINERAL ANA 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 1981-02-12 under 510(k) number K810140. 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 DUAL-PHOTON TOTAL BODY BONE MINERAL ANA?

DUAL-PHOTON TOTAL BODY BONE MINERAL ANA is a medical device that received FDA 510(k) clearance on 1981-02-12. The listed applicant is Lunar Radiation Corp.. The 510(k) number is K810140.

When did DUAL-PHOTON TOTAL BODY BONE MINERAL ANA receive FDA 510(k) clearance?

DUAL-PHOTON TOTAL BODY BONE MINERAL ANA received FDA 510(k) clearance on 1981-02-12, under 510(k) number K810140.

Who is the listed applicant for DUAL-PHOTON TOTAL BODY BONE MINERAL ANA?

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 DUAL-PHOTON TOTAL BODY BONE MINERAL ANA?

The FDA product code for DUAL-PHOTON TOTAL BODY BONE MINERAL ANA is KGI.

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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 CONTROLLERK802180WISCONSIN DUAL-PHOTON BONE ANALYZERK802181WISCONSIN 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

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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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