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FDA 510(k)

ELECTRO-LUBE

K-Number: K033880 · 2004-03-10

ApplicantMectra Labs, Inc.
Decision Date2004-03-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO-LUBE is the device name listed in this FDA 510(k) record. The listed applicant is Mectra Labs, Inc.. It received FDA 510(k) clearance on 2004-03-10 under 510(k) number K033880. 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 ELECTRO-LUBE?

ELECTRO-LUBE is a medical device that received FDA 510(k) clearance on 2004-03-10. The listed applicant is Mectra Labs, Inc.. The 510(k) number is K033880.

When did ELECTRO-LUBE receive FDA 510(k) clearance?

ELECTRO-LUBE received FDA 510(k) clearance on 2004-03-10, under 510(k) number K033880.

Who is the listed applicant for ELECTRO-LUBE?

The FDA 510(k) record lists Mectra Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRO-LUBE?

The FDA product code for ELECTRO-LUBE is GEI.

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Other records listing Mectra Labs, Inc. as applicant

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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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