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)

MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY

K-Number: K827609 · 1982-07-09

ApplicantMidwest X-Ray Equipment Co.
Decision Date1982-07-09
Product Code
DecisionSubstantially Equivalent

Device Summary

MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Midwest X-Ray Equipment Co.. It received FDA 510(k) clearance on 1982-07-09 under 510(k) number K827609. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY?

MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Midwest X-Ray Equipment Co.. The 510(k) number is K827609.

When did MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY receive FDA 510(k) clearance?

MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY received FDA 510(k) clearance on 1982-07-09, under 510(k) number K827609.

Who is the listed applicant for MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY?

The FDA 510(k) record lists Midwest X-Ray Equipment Co. 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 Midwest X-Ray Equipment Co. 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.

K924423MWX-7440 HIGH SPEED BUCKYK827504SIZE SENSING CASSETTE TRAY

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.

↑