510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K911104Substantially Equivalent

Photcoagulator Kr-568 Laser Spectrum Elite K1

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

K911104 is the FDA 510(k) clearance record for PHOTCOAGULATOR KR-568 LASER SPECTRUM ELITE K1, a class I device, cleared for Hgm Medical Laser Systems, Inc. on under FDA product code FEX (Instrument, Catheter, Punch). FDA records list 18 510(k) clearances for Hgm Medical Laser Systems, Inc., from to . As of , FDA records show no recalls naming K911104.

Clearance record

Decision date
Received
(90 days to decision)
Product code
FEX Instrument, Catheter, Punch
Regulation
21 CFR 876.5090
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Hgm Medical Laser Systems, Inc. 3959 W. 1820 S., Salt Lake City UT
Third party review
No

Clearances, product code FEX

Trailing 12 months

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

FDA records show no clearances under product code FEX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FEX, 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