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FDA 510(k)

GE CT/T MODEL NO. B7800 A

K-Number: K760882 · 1976-11-19

ApplicantArnold & Porter For G.E. Co.
Decision Date1976-11-19
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE CT/T MODEL NO. B7800 A is the device name listed in this FDA 510(k) record. The listed applicant is Arnold & Porter For G.E. Co.. It received FDA 510(k) clearance on 1976-11-19 under 510(k) number K760882. 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 GE CT/T MODEL NO. B7800 A?

GE CT/T MODEL NO. B7800 A is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is Arnold & Porter For G.E. Co.. The 510(k) number is K760882.

When did GE CT/T MODEL NO. B7800 A receive FDA 510(k) clearance?

GE CT/T MODEL NO. B7800 A received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760882.

Who is the listed applicant for GE CT/T MODEL NO. B7800 A?

The FDA 510(k) record lists Arnold & Porter For G.E. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GE CT/T MODEL NO. B7800 A?

The FDA product code for GE CT/T MODEL NO. B7800 A is JAK.

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Related Devices (Code: JAK)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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