SOL-CARE SAFETY NEEDLE— 510(k) K123684

Substantially Equivalent

Sol-Millennium Medical

FDA 510(k) clearance K123684 for SOL-CARE SAFETY NEEDLE, Substantially Equivalent on 2013-05-08. Applicant: Sol-Millennium Medical. Device class: 2.

Clearance details

Applicant
Sol-Millennium Medical
Product code
Code FMI
Device class
Class 2
Regulation
21 CFR 880.5570
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lawrenceville, GA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code FMI

view all

Adverse events under product code FMI

product code FMI
Death
28
Injury
1,517
Malfunction
23,981
Other
18
Total
25,544

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 →

Recalls naming K123684

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K123684.

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