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

Laser, Microsurgical Argon, For Uses Other Than Otology, Including Laryngology & General Use In Otolaryngology

21 CFR 874.4490 / Ear, Nose, Throat
FDA source (opens on fda.gov)

LMS is the FDA product code for Laser, Microsurgical Argon, For Uses Other Than Otology, Including Laryngology & General Use In Otolaryngology, a class II device type, regulated under 21 CFR 874.4490. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LMS
Device name
Laser, Microsurgical Argon, For Uses Other Than Otology, Including Laryngology & General Use In Otolaryngology
Regulation
21 CFR 874.4490
Device class
Class II
Review panel
Ear, Nose, Throat
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code LMS

By decision year
2 clearances under product code LMS with a decision year between 1986 and 1987, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LMS by decision year
YearClearances
19861
19871

Applicants with the most clearances

Product code LMS
Applicants holding the most 510(k) clearances under product code LMS
ApplicantClearances
Hgm, Inc.1
Laserscope1

Companies listing this code with FDA

Companies whose registered establishments list this code

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