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FDA 510(k)

VL7600 REM PATIENT RETURN ELECTRODE

K-Number: K953737 · 1995-08-23

ApplicantValleylab, Inc.
Decision Date1995-08-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VL7600 REM PATIENT RETURN ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1995-08-23 under 510(k) number K953737. 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 VL7600 REM PATIENT RETURN ELECTRODE?

VL7600 REM PATIENT RETURN ELECTRODE is a medical device that received FDA 510(k) clearance on 1995-08-23. The listed applicant is Valleylab, Inc.. The 510(k) number is K953737.

When did VL7600 REM PATIENT RETURN ELECTRODE receive FDA 510(k) clearance?

VL7600 REM PATIENT RETURN ELECTRODE received FDA 510(k) clearance on 1995-08-23, under 510(k) number K953737.

Who is the listed applicant for VL7600 REM PATIENT RETURN ELECTRODE?

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 VL7600 REM PATIENT RETURN ELECTRODE?

The FDA product code for VL7600 REM PATIENT RETURN ELECTRODE is GEI.

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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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