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FDA 510(k)

YESNG REUSABLE ELECTROSURGICAL HANDLE

K-Number: K881408 · 1988-04-14

Decision Date1988-04-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YESNG REUSABLE ELECTROSURGICAL HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K881408. 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 YESNG REUSABLE ELECTROSURGICAL HANDLE?

YESNG REUSABLE ELECTROSURGICAL HANDLE is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Ferguson Medical. The 510(k) number is K881408.

When did YESNG REUSABLE ELECTROSURGICAL HANDLE receive FDA 510(k) clearance?

YESNG REUSABLE ELECTROSURGICAL HANDLE received FDA 510(k) clearance on 1988-04-14, under 510(k) number K881408.

Who is the listed applicant for YESNG REUSABLE ELECTROSURGICAL HANDLE?

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

What is the FDA product code for YESNG REUSABLE ELECTROSURGICAL HANDLE?

The FDA product code for YESNG REUSABLE ELECTROSURGICAL HANDLE is GEI.

Related Clinical Trials

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.

Other records listing Ferguson Medical 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.

View all 57 devices →

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.

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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