510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K870587Substantially Equivalent for Some Indications

Lasermatic Surgilaser Model 5050

Lasermatic, Inc., Finland, FI / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K870587 is the FDA 510(k) clearance record for LASERMATIC SURGILASER MODEL 5050, a class II device, cleared for Lasermatic OY on under FDA product code EWG (Laser, Ent Microsurgical Carbon-Dioxide). FDA records list 10 510(k) clearances for Lasermatic OY, from to . As of , FDA records show no recalls naming K870587.

Clearance record

Decision date
Received
(547 days to decision)
Product code
EWG Laser, Ent Microsurgical Carbon-Dioxide
Regulation
21 CFR 874.4500
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Lasermatic OY Lepolantie 21, Finland, FI
Third party review
No

Clearances, product code EWG

Trailing 12 months

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

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