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)

DYNATRON 330 BODY COMPOSITION ANALYZER

K-Number: K900321 · 1990-06-11

ApplicantDynatronics Laser Corp.
Decision Date1990-06-11
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DYNATRON 330 BODY COMPOSITION ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Laser Corp.. It received FDA 510(k) clearance on 1990-06-11 under 510(k) number K900321. 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 DYNATRON 330 BODY COMPOSITION ANALYZER?

DYNATRON 330 BODY COMPOSITION ANALYZER is a medical device that received FDA 510(k) clearance on 1990-06-11. The listed applicant is Dynatronics Laser Corp.. The 510(k) number is K900321.

When did DYNATRON 330 BODY COMPOSITION ANALYZER receive FDA 510(k) clearance?

DYNATRON 330 BODY COMPOSITION ANALYZER received FDA 510(k) clearance on 1990-06-11, under 510(k) number K900321.

Who is the listed applicant for DYNATRON 330 BODY COMPOSITION ANALYZER?

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

What is the FDA product code for DYNATRON 330 BODY COMPOSITION ANALYZER?

The FDA product code for DYNATRON 330 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

Other records listing Dynatronics Laser 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.

K920939DYNATRON 300 ULRASOUNDK900639DYNATRON 350 EMG/BIOFEEDBACK ANALYZERK880464DYNATRON IIK864370DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)

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.

↑