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FDA 510(k)

LINEAR ARRAY B-MODE SCANNER

K-Number: K771934 · 1977-10-25

ApplicantG.D. Searle and Co.
Decision Date1977-10-25
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LINEAR ARRAY B-MODE SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771934. 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 ARRAY B-MODE SCANNER?

LINEAR ARRAY B-MODE SCANNER is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is G.D. Searle and Co.. The 510(k) number is K771934.

When did LINEAR ARRAY B-MODE SCANNER receive FDA 510(k) clearance?

LINEAR ARRAY B-MODE SCANNER received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771934.

Who is the listed applicant for LINEAR ARRAY B-MODE SCANNER?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINEAR ARRAY B-MODE SCANNER?

The FDA product code for LINEAR ARRAY B-MODE SCANNER is IYO.

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Other records listing G.D. Searle and Co. as applicant

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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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