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FDA 510(k)

ADMINISTRATION SET

K-Number: K810131 · 1981-02-26

ApplicantG.D. Searle and Co.
Decision Date1981-02-26
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADMINISTRATION SET 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 1981-02-26 under 510(k) number K810131. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADMINISTRATION SET?

ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is G.D. Searle and Co.. The 510(k) number is K810131.

When did ADMINISTRATION SET receive FDA 510(k) clearance?

ADMINISTRATION SET received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810131.

Who is the listed applicant for ADMINISTRATION SET?

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 ADMINISTRATION SET?

The FDA product code for ADMINISTRATION SET is FPD.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: FPD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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