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FDA 510(k)

VALLEYLAB RETRACTABLE ELECTRODES

K-Number: K931028 · 1993-07-27

ApplicantValleylab, Inc.
Decision Date1993-07-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEYLAB RETRACTABLE ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K931028. 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 VALLEYLAB RETRACTABLE ELECTRODES?

VALLEYLAB RETRACTABLE ELECTRODES is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Valleylab, Inc.. The 510(k) number is K931028.

When did VALLEYLAB RETRACTABLE ELECTRODES receive FDA 510(k) clearance?

VALLEYLAB RETRACTABLE ELECTRODES received FDA 510(k) clearance on 1993-07-27, under 510(k) number K931028.

Who is the listed applicant for VALLEYLAB RETRACTABLE ELECTRODES?

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 VALLEYLAB RETRACTABLE ELECTRODES?

The FDA product code for VALLEYLAB RETRACTABLE ELECTRODES is GEI.

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Other records listing Valleylab, 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.

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Related Devices (Code: 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.

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