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FDA 510(k)

PALOMAR LIGHTCUBE

K-Number: K024179 · 2003-06-04

ApplicantPalomar Medical Products, Inc.
Decision Date2003-06-04
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PALOMAR LIGHTCUBE is the device name listed in this FDA 510(k) record. The listed applicant is Palomar Medical Products, Inc.. It received FDA 510(k) clearance on 2003-06-04 under 510(k) number K024179. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALOMAR LIGHTCUBE?

PALOMAR LIGHTCUBE is a medical device that received FDA 510(k) clearance on 2003-06-04. The listed applicant is Palomar Medical Products, Inc.. The 510(k) number is K024179.

When did PALOMAR LIGHTCUBE receive FDA 510(k) clearance?

PALOMAR LIGHTCUBE received FDA 510(k) clearance on 2003-06-04, under 510(k) number K024179.

Who is the listed applicant for PALOMAR LIGHTCUBE?

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

What is the FDA product code for PALOMAR LIGHTCUBE?

The FDA product code for PALOMAR LIGHTCUBE is ILY.

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Other records listing Palomar Medical Products, Inc. as applicant

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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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