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)

MODIFICATION TO ACCUDEXA BONE DENSITOMETER

K-Number: K001429 · 2000-05-26

ApplicantSchick Technologies, Inc.
Decision Date2000-05-26
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO ACCUDEXA BONE DENSITOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Schick Technologies, Inc.. It received FDA 510(k) clearance on 2000-05-26 under 510(k) number K001429. 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 MODIFICATION TO ACCUDEXA BONE DENSITOMETER?

MODIFICATION TO ACCUDEXA BONE DENSITOMETER is a medical device that received FDA 510(k) clearance on 2000-05-26. The listed applicant is Schick Technologies, Inc.. The 510(k) number is K001429.

When did MODIFICATION TO ACCUDEXA BONE DENSITOMETER receive FDA 510(k) clearance?

MODIFICATION TO ACCUDEXA BONE DENSITOMETER received FDA 510(k) clearance on 2000-05-26, under 510(k) number K001429.

Who is the listed applicant for MODIFICATION TO ACCUDEXA BONE DENSITOMETER?

The FDA 510(k) record lists Schick Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO ACCUDEXA BONE DENSITOMETER?

The FDA product code for MODIFICATION TO ACCUDEXA 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 Schick Technologies, Inc. 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.

K110768COMPUTED DENTAL RADIOGRAPHYK093453MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMK072134SCHICK COMPUTED ORAL RADIOLOGY SYSTEMK053558CEPH, MODEL 4900K041385MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMK031291CDR PANX, MODEL 4792

View all 13 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.

↑