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FDA 510(k)

MODEL E2510 SURGISWITCH

K-Number: K791638 · 1979-09-12

ApplicantValleylab, Inc.
Decision Date1979-09-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL E2510 SURGISWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1979-09-12 under 510(k) number K791638. 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 MODEL E2510 SURGISWITCH?

MODEL E2510 SURGISWITCH is a medical device that received FDA 510(k) clearance on 1979-09-12. The listed applicant is Valleylab, Inc.. The 510(k) number is K791638.

When did MODEL E2510 SURGISWITCH receive FDA 510(k) clearance?

MODEL E2510 SURGISWITCH received FDA 510(k) clearance on 1979-09-12, under 510(k) number K791638.

Who is the listed applicant for MODEL E2510 SURGISWITCH?

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 MODEL E2510 SURGISWITCH?

The FDA product code for MODEL E2510 SURGISWITCH is GEI.

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Related Devices (Code: GEI)

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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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