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FDA 510(k)

LEY ELECTRO-SURGICAL UNITS

K-Number: K790642 · 1979-05-08

ApplicantMerced Medical, Inc.
Decision Date1979-05-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEY ELECTRO-SURGICAL UNITS is the device name listed in this FDA 510(k) record. The listed applicant is Merced Medical, Inc.. It received FDA 510(k) clearance on 1979-05-08 under 510(k) number K790642. 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 LEY ELECTRO-SURGICAL UNITS?

LEY ELECTRO-SURGICAL UNITS is a medical device that received FDA 510(k) clearance on 1979-05-08. The listed applicant is Merced Medical, Inc.. The 510(k) number is K790642.

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

LEY ELECTRO-SURGICAL UNITS received FDA 510(k) clearance on 1979-05-08, under 510(k) number K790642.

Who is the listed applicant for LEY ELECTRO-SURGICAL UNITS?

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

What is the FDA product code for LEY ELECTRO-SURGICAL UNITS?

The FDA product code for LEY ELECTRO-SURGICAL UNITS is GEI.

Related Clinical Trials

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Other records listing Merced Medical, Inc. 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.

K915810MER BAGK911622CPR BAGK900569THERMOPROBE 210K901026MJ PERCUSSOR(TM)

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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