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FDA 510(k)

MWX-7440 HIGH SPEED BUCKY

K-Number: K924423 · 1993-01-15

ApplicantMidwest X-Ray Equipment Co.
Decision Date1993-01-15
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MWX-7440 HIGH SPEED BUCKY 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 1993-01-15 under 510(k) number K924423. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MWX-7440 HIGH SPEED BUCKY?

MWX-7440 HIGH SPEED BUCKY is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Midwest X-Ray Equipment Co.. The 510(k) number is K924423.

When did MWX-7440 HIGH SPEED BUCKY receive FDA 510(k) clearance?

MWX-7440 HIGH SPEED BUCKY received FDA 510(k) clearance on 1993-01-15, under 510(k) number K924423.

Who is the listed applicant for MWX-7440 HIGH SPEED BUCKY?

The FDA 510(k) record lists Midwest X-Ray Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MWX-7440 HIGH SPEED BUCKY?

The FDA product code for MWX-7440 HIGH SPEED BUCKY is KPX.

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.

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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.

K827609MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAYK827504SIZE SENSING CASSETTE TRAY

Related Devices (Code: KPX)

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.

K945635TRANS X-1000Canon USA, Inc.K935157ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBESRegulatory Consultants TO the Medical Device IndusK934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSVictoreen, Inc.K933035BCM-600TXB C Medical , Ltd.K925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGERAcoma Medical Imaging, Inc.K925169SHIMADZU RADIOGRAPJHIC STAND BR-100Shimadzu Medical Systems

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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