FDA 510(k)

E2508 DISPOSABLE HANDSWITCHING PENCIL

K-Number: K813071 · 1981-11-10

Decision Date1981-11-10

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

E2508 DISPOSABLE HANDSWITCHING PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K813071. 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 E2508 DISPOSABLE HANDSWITCHING PENCIL?

E2508 DISPOSABLE HANDSWITCHING PENCIL is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is Valleylab, Inc.. The 510(k) number is K813071.

When did E2508 DISPOSABLE HANDSWITCHING PENCIL receive FDA 510(k) clearance?

E2508 DISPOSABLE HANDSWITCHING PENCIL received FDA 510(k) clearance on 1981-11-10, under 510(k) number K813071.

Who is the listed applicant for E2508 DISPOSABLE HANDSWITCHING PENCIL?

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 E2508 DISPOSABLE HANDSWITCHING PENCIL?

The FDA product code for E2508 DISPOSABLE HANDSWITCHING PENCIL is 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.