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FDA 510(k)

BONE MINERAL ANALYZER CONTROLLER

K-Number: K810159 · 1981-02-12

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

Device Summary

BONE MINERAL ANALYZER CONTROLLER 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 K810159. 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 BONE MINERAL ANALYZER CONTROLLER?

BONE MINERAL ANALYZER CONTROLLER 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 K810159.

When did BONE MINERAL ANALYZER CONTROLLER receive FDA 510(k) clearance?

BONE MINERAL ANALYZER CONTROLLER received FDA 510(k) clearance on 1981-02-12, under 510(k) number K810159.

Who is the listed applicant for BONE MINERAL ANALYZER CONTROLLER?

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 BONE MINERAL ANALYZER CONTROLLER?

The FDA product code for BONE MINERAL ANALYZER CONTROLLER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 DENSITOMETERK810140DUAL-PHOTON TOTAL BODY BONE MINERAL ANAK802180WISCONSIN 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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