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

Cleaners, Medical Devices

21 CFR 880.6992 / General Hospital
FDA source (opens on fda.gov)

MDZ is the FDA product code for Cleaners, Medical Devices, a class II device type, regulated under 21 CFR 880.6992. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
MDZ
Device name
Cleaners, Medical Devices
Regulation
21 CFR 880.6992
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
Yes
Ingested clearances
2
Ingested recalls
2

Clearances, product code MDZ

By decision year
2 clearances under product code MDZ with a decision year between 1994 and 1994, 1994 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MDZ by decision year
YearClearances
19942

Applicants with the most clearances

Product code MDZ
Applicants holding the most 510(k) clearances under product code MDZ
ApplicantClearances
Getinge International, Inc.2

Companies listing this code with FDA

Companies whose registered establishments list this code