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FDA 510(k)

LINEAR SCANNER 640

K-Number: K840667 · 1984-04-23

ApplicantGe Medical Systems Information Technologies
Decision Date1984-04-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LINEAR SCANNER 640 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K840667. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEAR SCANNER 640?

LINEAR SCANNER 640 is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K840667.

When did LINEAR SCANNER 640 receive FDA 510(k) clearance?

LINEAR SCANNER 640 received FDA 510(k) clearance on 1984-04-23, under 510(k) number K840667.

Who is the listed applicant for LINEAR SCANNER 640?

The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINEAR SCANNER 640?

The FDA product code for LINEAR SCANNER 640 is IYO.

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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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