FDA 510(k)

DISPOSABLE LECTROSWITCH, MODEL E2503

K-Number: K781510 · 1978-10-24

Decision Date1978-10-24

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

DISPOSABLE LECTROSWITCH, MODEL E2503 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1978-10-24 under 510(k) number K781510. 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 DISPOSABLE LECTROSWITCH, MODEL E2503?

DISPOSABLE LECTROSWITCH, MODEL E2503 is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is Valleylab, Inc.. The 510(k) number is K781510.

When did DISPOSABLE LECTROSWITCH, MODEL E2503 receive FDA 510(k) clearance?

DISPOSABLE LECTROSWITCH, MODEL E2503 received FDA 510(k) clearance on 1978-10-24, under 510(k) number K781510.

Who is the listed applicant for DISPOSABLE LECTROSWITCH, MODEL E2503?

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

What is the FDA product code for DISPOSABLE LECTROSWITCH, MODEL E2503?

The FDA product code for DISPOSABLE LECTROSWITCH, MODEL E2503 is GEI.

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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.