FDA 510(k)

MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS

K-Number: K914400 · 1991-10-17

Decision Date1991-10-17

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1991-10-17 under 510(k) number K914400. 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 MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS?

MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS is a medical device that received FDA 510(k) clearance on 1991-10-17. The listed applicant is Valleylab, Inc.. The 510(k) number is K914400.

When did MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS receive FDA 510(k) clearance?

MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS received FDA 510(k) clearance on 1991-10-17, under 510(k) number K914400.

Who is the listed applicant for MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS?

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 MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS?

The FDA product code for MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS 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.