Product code MMK— General Hospital

SHARPS CONTAINER

Classification name
Container, Sharps
Device class
Class 2
Regulation
21 CFR 880.5570
Advisory panel
General Hospital
Total cleared
114
First cleared
Most recent

Market context for product code MMK

FDA has cleared 114 devices under product code MMK between 1977 and 2026, filed by 79 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code MMK

Recent clearances under product code MMK

1–100 of 114

Data sourced from openFDA. This site is unofficial and independent of the FDA.