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FDA 510(k)

UNIVERSAL STAND FOR FILM CHANGER

K-Number: K862575 · 1986-07-14

ApplicantCanon USA, Inc.
Decision Date1986-07-14
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL STAND FOR FILM CHANGER is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 1986-07-14 under 510(k) number K862575. 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 UNIVERSAL STAND FOR FILM CHANGER?

UNIVERSAL STAND FOR FILM CHANGER is a medical device that received FDA 510(k) clearance on 1986-07-14. The listed applicant is Canon USA, Inc.. The 510(k) number is K862575.

When did UNIVERSAL STAND FOR FILM CHANGER receive FDA 510(k) clearance?

UNIVERSAL STAND FOR FILM CHANGER received FDA 510(k) clearance on 1986-07-14, under 510(k) number K862575.

Who is the listed applicant for UNIVERSAL STAND FOR FILM CHANGER?

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

What is the FDA product code for UNIVERSAL STAND FOR FILM CHANGER?

The FDA product code for UNIVERSAL STAND FOR FILM CHANGER is KPX.

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Other records listing Canon USA, 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.

K090623DIGITAL RADIOGRAPHY CXDI-40G COMPACTK033624PACS SOFTWARE SOLUTION 2003K031633CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40CK031629CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGIK023750CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40GK023586DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS

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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.K925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGERAcoma Medical Imaging, Inc.K924423MWX-7440 HIGH SPEED BUCKYMidwest X-Ray Equipment Co.

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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