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

Fluidic, Phacoemulsification/Phacofragmentation

21 CFR 886.4670 / Ophthalmic
FDA source (opens on fda.gov)

MUS is the FDA product code for Fluidic, Phacoemulsification/Phacofragmentation, a class II device type, regulated under 21 CFR 886.4670. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MUS
Device name
Fluidic, Phacoemulsification/Phacofragmentation
Regulation
21 CFR 886.4670
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code MUS

By decision year
1 clearance under product code MUS with a decision year between 1998 and 1998, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MUS by decision year
YearClearances
19981

Applicants with the most clearances

Product code MUS
Applicants holding the most 510(k) clearances under product code MUS
ApplicantClearances
Alcon Laboratories1

Companies listing this code with FDA

Companies whose registered establishments list this code

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