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FDA 510(k)

MAXICAMERA 400T W/BODY CONTOUR TOMOGRA

K-Number: K841996 · 1984-07-16

ApplicantGeneral Electric Co.
Decision Date1984-07-16
Product CodeJAM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAXICAMERA 400T W/BODY CONTOUR TOMOGRA is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1984-07-16 under 510(k) number K841996. The device is classified under product code JAM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXICAMERA 400T W/BODY CONTOUR TOMOGRA?

MAXICAMERA 400T W/BODY CONTOUR TOMOGRA is a medical device that received FDA 510(k) clearance on 1984-07-16. The listed applicant is General Electric Co.. The 510(k) number is K841996.

When did MAXICAMERA 400T W/BODY CONTOUR TOMOGRA receive FDA 510(k) clearance?

MAXICAMERA 400T W/BODY CONTOUR TOMOGRA received FDA 510(k) clearance on 1984-07-16, under 510(k) number K841996.

Who is the listed applicant for MAXICAMERA 400T W/BODY CONTOUR TOMOGRA?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAXICAMERA 400T W/BODY CONTOUR TOMOGRA?

The FDA product code for MAXICAMERA 400T W/BODY CONTOUR TOMOGRA is JAM.

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Related Devices (Code: JAM)

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.

K842895WBA - I.R.I.S.Siemens Gammasonics, Inc.K770530CLEON IMAGERUnion Carbide Corp.

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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