Endocoagulator Models 8 and 20 Argon Laser

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K873773 ↗

FDA Product Code

GEX

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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See all devices from Hgm, Inc. →

• What is the Endocoagulator Models 8 and 20 Argon Laser used for?

  The Endocoagulator Models 8 and 20 Argon Laser is a medical device designed for coagulation procedures during surgical interventions. It utilizes argon laser technology to perform tissue coagulation specifically in general and plastic surgery settings.

• What is the regulatory status of this device?

  The Endocoagulator Models 8 and 20 Argon Laser has received FDA 510(k) clearance with number K873773. It is classified under product code GEX and was determined to be substantially equivalent to predicate devices.

• How is the Endocoagulator supplied?

  The Endocoagulator Models 8 and 20 Argon Laser is supplied by Hgm, Inc., a medical device manufacturer based in Salt Lake City, Utah. The device is provided as a complete system for use in surgical procedures requiring tissue coagulation.

• What are the intended applications of this device?

  This device is specifically intended for use in general and plastic surgery settings where tissue coagulation is required. It utilizes argon laser technology to perform coagulation procedures during various surgical interventions.