Product code MEG— General Hospital

DUOPRO SAFETY SYRINGE (DUOPROSS)

Classification name
Syringe, Antistick
Device class
Class 2
Regulation
21 CFR 880.5860
Advisory panel
General Hospital
Total cleared
163
First cleared
Most recent

Market context for product code MEG

FDA has cleared 163 devices under product code MEG between 1994 and 2026, filed by 109 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 MEG

Adverse events under product code MEG

product code MEG
Malfunction
1,373
Other
1
Total
1,374

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code MEG

1–100 of 163

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