510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
MXGClass II

Lamp, Uvc, (For Treating Skin And Wounds)

21 CFR 878.4630 / General, Plastic Surgery
FDA source (opens on fda.gov)

MXG is the FDA product code for Lamp, Uvc, (For Treating Skin And Wounds), a class II device type, regulated under 21 CFR 878.4630. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
MXG
Device name
Lamp, Uvc, (For Treating Skin And Wounds)
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
1

Clearances, product code MXG

By decision year
1 clearance under product code MXG with a decision year between 1999 and 1999, 1999 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MXG by decision year
YearClearances
19991

Applicants with the most clearances

Product code MXG
Applicants holding the most 510(k) clearances under product code MXG
ApplicantClearances
Medfaxx, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code