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FDA 510(k)

CT MAX, CATALOG NO. B7940 HA

K-Number: K862317 · 1986-10-07

ApplicantGeneral Electric Co.
Decision Date1986-10-07
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT MAX, CATALOG NO. B7940 HA 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 1986-10-07 under 510(k) number K862317. 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 CT MAX, CATALOG NO. B7940 HA?

CT MAX, CATALOG NO. B7940 HA is a medical device that received FDA 510(k) clearance on 1986-10-07. The listed applicant is General Electric Co.. The 510(k) number is K862317.

When did CT MAX, CATALOG NO. B7940 HA receive FDA 510(k) clearance?

CT MAX, CATALOG NO. B7940 HA received FDA 510(k) clearance on 1986-10-07, under 510(k) number K862317.

Who is the listed applicant for CT MAX, CATALOG NO. B7940 HA?

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 CT MAX, CATALOG NO. B7940 HA?

The FDA product code for CT MAX, CATALOG NO. B7940 HA 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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