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)

ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC

K-Number: K828051 · 1982-09-29

ApplicantAdr Ultrasound
Decision Date1982-09-29
Product Code
DecisionSubstantially Equivalent

Device Summary

ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC is the device name listed in this FDA 510(k) record. The listed applicant is Adr Ultrasound. It received FDA 510(k) clearance on 1982-09-29 under 510(k) number K828051. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC?

ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC is a medical device that received FDA 510(k) clearance on 1982-09-29. The listed applicant is Adr Ultrasound. The 510(k) number is K828051.

When did ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC receive FDA 510(k) clearance?

ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC received FDA 510(k) clearance on 1982-09-29, under 510(k) number K828051.

Who is the listed applicant for ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC?

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

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 Adr Ultrasound 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.

K840408LINEAR ARRAY TRANSDUCER OR SCANHEADK834141ULTRASOUND SCAN HEAD 3.5 MHZK833224BIFOCAL 3.0MHZK828053ADR ULTRASOUND 5.5 MHZ SHORT FOCUS TRANSDUCERK828050ADR ULTRASOUND MODEL 4000 LK828049ADR ULTRASOUND MC2 LARGE CART

View all 10 devices →

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.

↑