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FDA Product Code

FDA Product Code FMK — Clearance Directory

Device Class
Class II
21 CFR Citation
878.4850

510(k) Clearances — 111 records · page 2 of 2

K-Number Device Name Applicant Decision Date Clearance Type Summary
K833816 HEMASTICK 1-1.5 & 2-DISPOS. BLOOD Medprobe Laboratories 1983-12-22 Traditional PDF ↗
K833812 SUPERJET DISPOSABLE BLOOD LANCET Medrobe Laboratories 1983-12-12 Traditional PDF ↗
K833344 AUTO-LANCET Palco Laboratories, Inc. 1983-11-07 Traditional PDF ↗
K830001 SUPERJET BTD BLEEDING TIME DEVICE DISP Medprobe Laboratories 1983-09-26 Traditional PDF ↗
K830010 SUPERJET LANCET Medprobe Laboratories 1983-01-26 Traditional PDF ↗
K823760 PRICK-TEST NEEDLE Cordis Corp. 1983-01-14 Traditional PDF ↗
K822209 AUTOLANCET Bd Becton Dickinson Vacutainer Systems Preanalytic 1982-08-27 Traditional PDF ↗
K820625 HEMALET AUTOMATIC LANCET DEVICE Medprobe Laboratories 1982-04-09 Traditional PDF ↗
K820333 MONOJECTOR MONOLET LANCER Sherwood Medical Co. 1982-03-10 Traditional PDF ↗
K810681 MEDI-LANCE Medicore, Inc. 1981-03-26 Traditional PDF ↗
K810075 AUTOCLIX Biodynamics Corp. 1981-02-04 Traditional PDF ↗

Product code FMK · Class II · General, Plastic Surgery. Data: openFDA.