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FDA 510(k)

ELECTRODE, MODEL E7504 PREP II

K-Number: K790296 · 1979-04-12

ApplicantValleylab, Inc.
Decision Date1979-04-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRODE, MODEL E7504 PREP II is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1979-04-12 under 510(k) number K790296. 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 ELECTRODE, MODEL E7504 PREP II?

ELECTRODE, MODEL E7504 PREP II is a medical device that received FDA 510(k) clearance on 1979-04-12. The listed applicant is Valleylab, Inc.. The 510(k) number is K790296.

When did ELECTRODE, MODEL E7504 PREP II receive FDA 510(k) clearance?

ELECTRODE, MODEL E7504 PREP II received FDA 510(k) clearance on 1979-04-12, under 510(k) number K790296.

Who is the listed applicant for ELECTRODE, MODEL E7504 PREP II?

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 ELECTRODE, MODEL E7504 PREP II?

The FDA product code for ELECTRODE, MODEL E7504 PREP II 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.

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