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FDA 510(k)

LLOYD LINDEN, MODEL E04

K-Number: K071761 · 2007-08-03

ApplicantLloyd Linden, Inc.
Decision Date2007-08-03
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LLOYD LINDEN, MODEL E04 is the device name listed in this FDA 510(k) record. The listed applicant is Lloyd Linden, Inc.. It received FDA 510(k) clearance on 2007-08-03 under 510(k) number K071761. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LLOYD LINDEN, MODEL E04?

LLOYD LINDEN, MODEL E04 is a medical device that received FDA 510(k) clearance on 2007-08-03. The listed applicant is Lloyd Linden, Inc.. The 510(k) number is K071761.

When did LLOYD LINDEN, MODEL E04 receive FDA 510(k) clearance?

LLOYD LINDEN, MODEL E04 received FDA 510(k) clearance on 2007-08-03, under 510(k) number K071761.

Who is the listed applicant for LLOYD LINDEN, MODEL E04?

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

What is the FDA product code for LLOYD LINDEN, MODEL E04?

The FDA product code for LLOYD LINDEN, MODEL E04 is IPL.

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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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