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

Dressing, Compression

21 CFR 880.5075 / General Hospital
FDA source (opens on fda.gov)

MHW is the FDA product code for Dressing, Compression, a class I device type, regulated under 21 CFR 880.5075. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
MHW
Device name
Dressing, Compression
Regulation
21 CFR 880.5075
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
5

Clearances, product code MHW

By decision year
2 clearances under product code MHW with a decision year between 1991 and 2007, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MHW by decision year
YearClearances
19911
20071

Applicants with the most clearances

Product code MHW
Applicants holding the most 510(k) clearances under product code MHW
ApplicantClearances
Arch Development Group1
Sun-Scientific Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 226 companies shown, in name order