Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER

K-Number: K980125 · 1998-05-20

ApplicantNorland Corp.
Decision Date1998-05-20
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Norland Corp.. It received FDA 510(k) clearance on 1998-05-20 under 510(k) number K980125. 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 REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER?

REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER is a medical device that received FDA 510(k) clearance on 1998-05-20. The listed applicant is Norland Corp.. The 510(k) number is K980125.

When did REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER receive FDA 510(k) clearance?

REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER received FDA 510(k) clearance on 1998-05-20, under 510(k) number K980125.

Who is the listed applicant for REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER?

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

What is the FDA product code for REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER?

The FDA product code for REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER 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 Norland 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.

K980569FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERSK980289FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETERK973459NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERSK973104NORLAND MODEL PDEXA BONE DENSITOMETERK972882APOLLOK931996MODEL PDEXA BONE DENSITOMETER

View all 15 devices →

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.

↑