FDA Product Code FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Single-use lancets with integrated sharps protection represent a significant advance in patient and healthcare worker safety. FDA product code FMK covers disposable blood lancets with integral sharps protection for single use.
These devices have a retractable or permanently shielded blade that is exposed only during the lancing action, preventing needle-stick injuries after use. They are used for capillary blood sampling in glucose monitoring and other point-of-care tests.
FMK devices are Class II medical devices, regulated under 21 CFR 878.4850 and reviewed by the FDA General & Plastic Surgery panel.
Leading manufacturers include Tianjin Huahong Technology Co., Ltd., Promisemed Hangzhou Meditech Co., Ltd. and Owen Mumford, Ltd..
109
Total
109
Cleared
91d
Avg days
1981
Since
109 devices
Cleared
Apr 30, 1986
DIALET LANCING DEVICE
Home Diagnostics, Inc.
General & Plastic Surgery
26d
Cleared
Apr 29, 1986
NEONATAL UNILET
Ulster Scientific, Inc.
General & Plastic Surgery
27d
Cleared
Apr 15, 1986
SUEL BLOOD LANCET
Exel Intl.
General & Plastic Surgery
20d
Cleared
Feb 11, 1986
GLUCOLET AUTOMATIC LANCING DEVICE FOR OBT. BLOOD
Miles Laboratories, Inc.
General & Plastic Surgery
47d
Cleared
Jan 03, 1986
CHURCHHILL LANCET
Churchill Corp.
General & Plastic Surgery
37d
Cleared
Jun 11, 1984
STERILE BLOOD LANCETS
Abco Dealers, Inc.
General & Plastic Surgery
49d
Cleared
Jan 14, 1983
PRICK-TEST NEEDLE
Cordis Corp.
General & Plastic Surgery
31d
Cleared
Aug 27, 1982
AUTOLANCET
Bd Becton Dickinson Vacutainer Systems Preanalytic
General & Plastic Surgery
32d
Cleared
Mar 10, 1982
MONOJECTOR MONOLET LANCER
Sherwood Medical Co.
General & Plastic Surgery
30d
Cleared
Feb 04, 1981
AUTOCLIX
Biodynamics Corp.
General & Plastic Surgery
22d