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FDA 510(k)

LECTROBRASIVE(R) E2401

K-Number: K882646 · 1988-07-18

ApplicantValleylab, Inc.
Decision Date1988-07-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LECTROBRASIVE(R) E2401 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K882646. 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 LECTROBRASIVE(R) E2401?

LECTROBRASIVE(R) E2401 is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Valleylab, Inc.. The 510(k) number is K882646.

When did LECTROBRASIVE(R) E2401 receive FDA 510(k) clearance?

LECTROBRASIVE(R) E2401 received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882646.

Who is the listed applicant for LECTROBRASIVE(R) E2401?

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 LECTROBRASIVE(R) E2401?

The FDA product code for LECTROBRASIVE(R) E2401 is GEI.

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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