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FDA 510(k)

HA-2 HUMAN BODY COMPOSITION ANALYZER

K-Number: K860749 · 1986-09-02

ApplicantDj Medical Instrument Corp. C/O Keller & Heckman
Decision Date1986-09-02
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HA-2 HUMAN BODY COMPOSITION ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Dj Medical Instrument Corp. C/O Keller & Heckman. It received FDA 510(k) clearance on 1986-09-02 under 510(k) number K860749. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HA-2 HUMAN BODY COMPOSITION ANALYZER?

HA-2 HUMAN BODY COMPOSITION ANALYZER is a medical device that received FDA 510(k) clearance on 1986-09-02. The listed applicant is Dj Medical Instrument Corp. C/O Keller & Heckman. The 510(k) number is K860749.

When did HA-2 HUMAN BODY COMPOSITION ANALYZER receive FDA 510(k) clearance?

HA-2 HUMAN BODY COMPOSITION ANALYZER received FDA 510(k) clearance on 1986-09-02, under 510(k) number K860749.

Who is the listed applicant for HA-2 HUMAN BODY COMPOSITION ANALYZER?

The FDA 510(k) record lists Dj Medical Instrument Corp. C/O Keller & Heckman as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HA-2 HUMAN BODY COMPOSITION ANALYZER?

The FDA product code for HA-2 HUMAN BODY COMPOSITION ANALYZER is DSB.

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

Related Devices (Code: DSB)

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.

K260224MySOZO Software version 6.1.0.1 (SW version 6.1.0.1)ImpediMed LimitedK250634BCM2-Body Composition MonitorFresenius Medical Care Renal Therapies Group, LLCK243727Re:BalansMode Sensors ASK250922Edema Guard Monitor (EGM) CardioSet-001Cardioset Medical , Ltd.K232089SOZO ProImpediMed LimitedK223217Zynex Monitoring System, Model CM-1600Zynex Medical, Inc.

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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