MVH — Device, Detection, Sulfide Class II

FDA Device Classification

FDA product code MVH covers "Device, Detection, Sulfide", a Class II medical device regulated under 21 CFR 872.1870. Submissions are reviewed by the Dental panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MVH
Device Class
Class II
Regulation Number
872.1870
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
DEN980003diamond general developmentDIAMOND PROBE/PERIO 2000 SYSTEMJuly 17, 1998