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

Pump, Infusion, Gallstone Dissolution

21 CFR 880.5725 / General Hospital
FDA source (opens on fda.gov)

MHD is the FDA product code for Pump, Infusion, Gallstone Dissolution, a class II device type, regulated under 21 CFR 880.5725. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MHD
Device name
Pump, Infusion, Gallstone Dissolution
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code MHD

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

Applicants with the most clearances

Product code MHD
Applicants holding the most 510(k) clearances under product code MHD
ApplicantClearances
Agilent Technologies, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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