Cooltouch Nd:Yag Laser System, Model Cooltouch, Cooltouch-Ii Nd:Yag Laser System, Model Cooltouch-Ii

FDA 510(k) K022817 · Icn Pharmaceuticals, Inc.

Substantially Equivalent

510(k) numberK022817

Submission

Device name
Cooltouch Nd:Yag Laser System, Model Cooltouch, Cooltouch-Ii Nd:Yag Laser System, Model Cooltouch-Ii
Applicant
Icn Pharmaceuticals, Inc.
Costa Mesa, CA, US
Received
August 26, 2002
Decision date
November 22, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEX – Powered Laser Surgical Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue, for general surgical purpose in medical specialties of general and plastic surgery, dermatology/aesthetic, podiatry, otolaryngology (ent), gynecology…

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Questions and answers

When was Cooltouch Nd:Yag Laser System, Model Cooltouch, Cooltouch-Ii Nd:Yag Laser System, Model Cooltouch-Ii cleared by the FDA?

Cooltouch Nd:Yag Laser System, Model Cooltouch, Cooltouch-Ii Nd:Yag Laser System, Model Cooltouch-Ii (K022817) received a 510(k) decision of Substantially Equivalent on November 22, 2002, 88 days after the submission was received.

What is the product code of K022817?

The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.