meddevicedb.com FDA Device Reference

FDA Product Code

FDA Product Code HEI — Clearance Directory

Device Class
Class II
21 CFR Citation
884.2660

510(k) Clearances — 3 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K012003 DRG REACTION CHAMBER/SAFETY TIP Doctor'S Research Group, Inc. 2002-02-12 Traditional PDF ↗
K920985 SNOWDEN-PENCER IRRIGATION PUMP Snowden-Pencer 1992-06-09 Traditional PDF ↗
K910982 INNERVISION IRRIGATION PUMP M.D. Engineering, Inc. 1991-08-26 Traditional PDF ↗

Product code HEI · Class II · Obstetrics/Gynecology. Data: openFDA.