MDZ — Cleaners, Medical Devices Class II

FDA Device Classification

FDA product code MDZ covers "Cleaners, Medical Devices", a Class II medical device regulated under 21 CFR 880.6992. Submissions are reviewed by the General Hospital panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
MDZ
Device Class
Class II
Regulation Number
880.6992
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K920406getinge internationalDECOMAT 228April 5, 1994
K920413getinge internationalDECOMAT A 8666April 5, 1994