MLC — Monitor, St Segment Class II

FDA Device Classification

FDA product code MLC covers "Monitor, St Segment", a Class II medical device regulated under 21 CFR 870.2340. Submissions are reviewed by the Cardiovascular panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
MLC
Device Class
Class II
Regulation Number
870.2340
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K993826draeger medicalNARKOMED 6000March 23, 2000
K926099datascopeDATASCOPE 6000 MONITORAugust 6, 1993