Product code FMK— General, Plastic Surgery

Safety Lancet

Classification name: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Device class: Class 2
Regulation: 21 CFR 878.4850
Advisory panel: General, Plastic Surgery
Total cleared: 111
First cleared: 1981-02-04
Most recent: 2026-09-13

Clearances under product code FMK — page 2

101–111 of 111

K833816 — HEMASTICK 1-1.5 & 2-DISPOS. BLOODMedprobe Laboratories·1983-12-22
K833812 — SUPERJET DISPOSABLE BLOOD LANCETMedrobe Laboratories·1983-12-12
K833344 — AUTO-LANCETPalco Laboratories, Inc.·1983-11-07
K830001 — SUPERJET BTD BLEEDING TIME DEVICE DISPMedprobe Laboratories·1983-09-26
K830010 — SUPERJET LANCETMedprobe Laboratories·1983-01-26
K823760 — PRICK-TEST NEEDLECordis Corp.·1983-01-14
K822209 — AUTOLANCETBd Becton Dickinson Vacutainer Systems Preanalytic·1982-08-27
K820625 — HEMALET AUTOMATIC LANCET DEVICEMedprobe Laboratories·1982-04-09
K820333 — MONOJECTOR MONOLET LANCERSherwood Medical Co.·1982-03-10
K810681 — MEDI-LANCEMedicore, Inc.·1981-03-26
K810075 — AUTOCLIXBiodynamics Corp.·1981-02-04

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