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FDA 510(k)

WHITE KNIGHT BOVIE CORD/SUCTION TUBE

K-Number: K802213 · 1980-10-10

ApplicantG.D. Searle and Co.
Decision Date1980-10-10
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WHITE KNIGHT BOVIE CORD/SUCTION TUBE 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 1980-10-10 under 510(k) number K802213. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITE KNIGHT BOVIE CORD/SUCTION TUBE?

WHITE KNIGHT BOVIE CORD/SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is G.D. Searle and Co.. The 510(k) number is K802213.

When did WHITE KNIGHT BOVIE CORD/SUCTION TUBE receive FDA 510(k) clearance?

WHITE KNIGHT BOVIE CORD/SUCTION TUBE received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802213.

Who is the listed applicant for WHITE KNIGHT BOVIE CORD/SUCTION TUBE?

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 WHITE KNIGHT BOVIE CORD/SUCTION TUBE?

The FDA product code for WHITE KNIGHT BOVIE CORD/SUCTION TUBE is KKX.

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

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Related Devices (Code: KKX)

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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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