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FDA 510(k)

BUCKYMATIC AUTOMATIC CHEST FILM CHANGER

K-Number: K925598 · 1993-02-01

ApplicantAcoma Medical Imaging, Inc.
Decision Date1993-02-01
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BUCKYMATIC AUTOMATIC CHEST FILM CHANGER is the device name listed in this FDA 510(k) record. The listed applicant is Acoma Medical Imaging, Inc.. It received FDA 510(k) clearance on 1993-02-01 under 510(k) number K925598. 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 BUCKYMATIC AUTOMATIC CHEST FILM CHANGER?

BUCKYMATIC AUTOMATIC CHEST FILM CHANGER is a medical device that received FDA 510(k) clearance on 1993-02-01. The listed applicant is Acoma Medical Imaging, Inc.. The 510(k) number is K925598.

When did BUCKYMATIC AUTOMATIC CHEST FILM CHANGER receive FDA 510(k) clearance?

BUCKYMATIC AUTOMATIC CHEST FILM CHANGER received FDA 510(k) clearance on 1993-02-01, under 510(k) number K925598.

Who is the listed applicant for BUCKYMATIC AUTOMATIC CHEST FILM CHANGER?

The FDA 510(k) record lists Acoma Medical Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUCKYMATIC AUTOMATIC CHEST FILM CHANGER?

The FDA product code for BUCKYMATIC AUTOMATIC CHEST FILM CHANGER is KPX.

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Other records listing Acoma Medical Imaging, Inc. 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.

K981227SYMPHONY 360 REMOTE CONTROL TABLEK981131PATHFINDER MOBILE C ARMK963851TILTING RADIOGRAPHIC TABLE (REMOTE)K944952ANGIOGRAPHIC SYSTEMK941004CTS SYSTEMK941017F/C/W TUBESTAND

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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.K924423MWX-7440 HIGH SPEED BUCKYMidwest X-Ray Equipment Co.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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