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FDA 510(k)

VALLEYLAB RETURN ELECTRODE MONITOR

K-Number: K801153 · 1980-05-20

ApplicantValleylab, Inc.
Decision Date1980-05-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEYLAB RETURN ELECTRODE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K801153. 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 RETURN ELECTRODE MONITOR?

VALLEYLAB RETURN ELECTRODE MONITOR is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is Valleylab, Inc.. The 510(k) number is K801153.

When did VALLEYLAB RETURN ELECTRODE MONITOR receive FDA 510(k) clearance?

VALLEYLAB RETURN ELECTRODE MONITOR received FDA 510(k) clearance on 1980-05-20, under 510(k) number K801153.

Who is the listed applicant for VALLEYLAB RETURN ELECTRODE MONITOR?

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 RETURN ELECTRODE MONITOR?

The FDA product code for VALLEYLAB RETURN ELECTRODE MONITOR is GEI.

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Other records listing Valleylab, Inc. as applicant

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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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