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FDA 510(k)

CT9800 QUICK 3D #B7919DA

K-Number: K871859 · 1987-08-12

ApplicantGeneral Electric Co.
Decision Date1987-08-12
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT9800 QUICK 3D #B7919DA 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 1987-08-12 under 510(k) number K871859. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CT9800 QUICK 3D #B7919DA?

CT9800 QUICK 3D #B7919DA is a medical device that received FDA 510(k) clearance on 1987-08-12. The listed applicant is General Electric Co.. The 510(k) number is K871859.

When did CT9800 QUICK 3D #B7919DA receive FDA 510(k) clearance?

CT9800 QUICK 3D #B7919DA received FDA 510(k) clearance on 1987-08-12, under 510(k) number K871859.

Who is the listed applicant for CT9800 QUICK 3D #B7919DA?

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 CT9800 QUICK 3D #B7919DA?

The FDA product code for CT9800 QUICK 3D #B7919DA is JAK.

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Related Devices (Code: JAK)

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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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