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

System, Microwave, Hair Removal

21 CFR 878.4400 / General, Plastic Surgery
FDA source (opens on fda.gov)

MWY is the FDA product code for System, Microwave, Hair Removal, a class II device type, regulated under 21 CFR 878.4400. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MWY
Device name
System, Microwave, Hair Removal
Regulation
21 CFR 878.4400
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
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code MWY

By decision year
2 clearances under product code MWY with a decision year between 1999 and 2001, 1999 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MWY by decision year
YearClearances
19991
20011

Applicants with the most clearances

Product code MWY
Applicants holding the most 510(k) clearances under product code MWY
ApplicantClearances
Microwave Medical, Inc.1
Mw Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code