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FDA 510(k)

E600B FOOTSWITCH

K-Number: K874794 · 1987-12-14

ApplicantValleylab, Inc.
Decision Date1987-12-14
Product CodeBWA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

E600B FOOTSWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1987-12-14 under 510(k) number K874794. The device is classified under product code BWA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E600B FOOTSWITCH?

E600B FOOTSWITCH is a medical device that received FDA 510(k) clearance on 1987-12-14. The listed applicant is Valleylab, Inc.. The 510(k) number is K874794.

When did E600B FOOTSWITCH receive FDA 510(k) clearance?

E600B FOOTSWITCH received FDA 510(k) clearance on 1987-12-14, under 510(k) number K874794.

Who is the listed applicant for E600B FOOTSWITCH?

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 E600B FOOTSWITCH?

The FDA product code for E600B FOOTSWITCH is BWA.

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Other records listing Valleylab, Inc. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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