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FDA 510(k)

K.E.P. CONNECTOR AND CLIP

K-Number: K042900 · 2004-11-05

ApplicantK.E.P., LLC
Decision Date2004-11-05
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

K.E.P. CONNECTOR AND CLIP is the device name listed in this FDA 510(k) record. The listed applicant is K.E.P., LLC. It received FDA 510(k) clearance on 2004-11-05 under 510(k) number K042900. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K.E.P. CONNECTOR AND CLIP?

K.E.P. CONNECTOR AND CLIP is a medical device that received FDA 510(k) clearance on 2004-11-05. The listed applicant is K.E.P., LLC. The 510(k) number is K042900.

When did K.E.P. CONNECTOR AND CLIP receive FDA 510(k) clearance?

K.E.P. CONNECTOR AND CLIP received FDA 510(k) clearance on 2004-11-05, under 510(k) number K042900.

Who is the listed applicant for K.E.P. CONNECTOR AND CLIP?

The FDA 510(k) record lists K.E.P., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K.E.P. CONNECTOR AND CLIP?

The FDA product code for K.E.P. CONNECTOR AND CLIP is KDJ.

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Related Devices (Code: KDJ)

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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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