LLFClass III

Laser, Neurosurgical, Argon

Unknown

LLF is the FDA product code for Laser, Neurosurgical, Argon, a class III device type. As of 2026-09-10, FDA records hold 4 510(k) clearances under this code, the most recent dated 1987-07-10, and no recalls.

Classification record

Product code: LLF
Device name: Laser, Neurosurgical, Argon
Device class: Class III
Review panel: Unknown
Submission type: Contact ODE
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 4
Ingested recalls: 0

Clearances, product code LLF

By decision year

4 clearances under product code LLF with a decision year between 1984 and 1987, 1987 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code LLF by decision year
Year	Clearances
1984	1
1986	1
1987	2

Applicants with the most clearances

Product code LLF

Applicants holding the most 510(k) clearances under product code LLF
Applicant	Clearances
Britt Corp., Inc.	1
Cooper Medical, SRL	1
Hgm, Inc.	1
Inframed, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LLF.

Recent clearances

Product code LLF

Recent recalls

Product code LLF

FDA records show no recalls under product code LLF.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)