510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K870773Substantially Equivalent

Endocoagulator Models 5, 8 & 20 Argon Laser

Hgm, Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870773 is the FDA 510(k) clearance record for ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER, a class III device, cleared for Hgm, Inc. on under FDA product code LLF (Laser, Neurosurgical, Argon). FDA records list 21 510(k) clearances for Hgm, Inc., from to . As of , FDA records show no recalls naming K870773.

Clearance record

Decision date
Received
(134 days to decision)
Product code
LLF Laser, Neurosurgical, Argon
Device class
Class III
Review panel
Unknown
Applicant
Hgm, Inc. 3959 W. 1820 S., Salt Lake City UT
Third party review
No

Clearances, product code LLF

Trailing 12 months

FDA records hold no clearances under product code LLF in the trailing twelve months.

FDA records show no clearances under product code LLF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LLF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260