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FDA 510(k)

ARTICULATED ARM B-SCANNER

K-Number: K811426 · 1981-08-18

ApplicantGeneral Electric Co.
Decision Date1981-08-18
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTICULATED ARM B-SCANNER 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 1981-08-18 under 510(k) number K811426. 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 ARTICULATED ARM B-SCANNER?

ARTICULATED ARM B-SCANNER is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is General Electric Co.. The 510(k) number is K811426.

When did ARTICULATED ARM B-SCANNER receive FDA 510(k) clearance?

ARTICULATED ARM B-SCANNER received FDA 510(k) clearance on 1981-08-18, under 510(k) number K811426.

Who is the listed applicant for ARTICULATED ARM B-SCANNER?

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 ARTICULATED ARM B-SCANNER?

The FDA product code for ARTICULATED ARM B-SCANNER 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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