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FDA 510(k)

SEARLE PHO/SONIC ALPHA 2000

K-Number: K800139 · 1980-02-11

ApplicantG.D. Searle and Co.
Decision Date1980-02-11
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SEARLE PHO/SONIC ALPHA 2000 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 1980-02-11 under 510(k) number K800139. 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 SEARLE PHO/SONIC ALPHA 2000?

SEARLE PHO/SONIC ALPHA 2000 is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is G.D. Searle and Co.. The 510(k) number is K800139.

When did SEARLE PHO/SONIC ALPHA 2000 receive FDA 510(k) clearance?

SEARLE PHO/SONIC ALPHA 2000 received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800139.

Who is the listed applicant for SEARLE PHO/SONIC ALPHA 2000?

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 SEARLE PHO/SONIC ALPHA 2000?

The FDA product code for SEARLE PHO/SONIC ALPHA 2000 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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