510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K880170Substantially Equivalent

Model 4900 Nd:yag Laser for Pulmonary Obstructions

Cooper Lasersonics, Inc., Santa Clara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880170 is the FDA 510(k) clearance record for MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS, a class II device, cleared for Cooper Lasersonics, Inc. on under FDA product code LLO (Laser, Neodymium:Yag, Pulmonary Surgery). FDA records list 54 510(k) clearances for Cooper Lasersonics, Inc., from to . As of , FDA records show no recalls naming K880170.

Clearance record

Decision date
Received
(69 days to decision)
Product code
LLO Laser, Neodymium:Yag, Pulmonary Surgery
Regulation
21 CFR 874.4500
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Cooper Lasersonics, Inc. 3420 Central Expy. ., Santa Clara CA
Third party review
No

Clearances, product code LLO

Trailing 12 months

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

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