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FDA 510(k)

ELECTRO-SURGICAL DEVICES

K-Number: K771009 · 1977-07-13

ApplicantDeseret Pharmaceutical Co.
Decision Date1977-07-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO-SURGICAL DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Deseret Pharmaceutical Co.. It received FDA 510(k) clearance on 1977-07-13 under 510(k) number K771009. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-SURGICAL DEVICES?

ELECTRO-SURGICAL DEVICES is a medical device that received FDA 510(k) clearance on 1977-07-13. The listed applicant is Deseret Pharmaceutical Co.. The 510(k) number is K771009.

When did ELECTRO-SURGICAL DEVICES receive FDA 510(k) clearance?

ELECTRO-SURGICAL DEVICES received FDA 510(k) clearance on 1977-07-13, under 510(k) number K771009.

Who is the listed applicant for ELECTRO-SURGICAL DEVICES?

The FDA 510(k) record lists Deseret Pharmaceutical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRO-SURGICAL DEVICES?

The FDA product code for ELECTRO-SURGICAL DEVICES is GEI.

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Related Devices (Code: GEI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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