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FDA 510(k)

X-RAY FILM, CONVEY OR SYSTEM

K-Number: K760279 · 1976-08-13

ApplicantMallinckrodt Group, Inc.
Decision Date1976-08-13
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY FILM, CONVEY OR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1976-08-13 under 510(k) number K760279. 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 X-RAY FILM, CONVEY OR SYSTEM?

X-RAY FILM, CONVEY OR SYSTEM is a medical device that received FDA 510(k) clearance on 1976-08-13. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K760279.

When did X-RAY FILM, CONVEY OR SYSTEM receive FDA 510(k) clearance?

X-RAY FILM, CONVEY OR SYSTEM received FDA 510(k) clearance on 1976-08-13, under 510(k) number K760279.

Who is the listed applicant for X-RAY FILM, CONVEY OR SYSTEM?

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

What is the FDA product code for X-RAY FILM, CONVEY OR SYSTEM?

The FDA product code for X-RAY FILM, CONVEY OR SYSTEM is KPX.

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Other records listing Mallinckrodt Group, Inc. as applicant

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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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