meddevicedb.com FDA Device Reference

FDA Product Code

FDA Product Code FIW — Clearance Directory

Device Class
Class II
21 CFR Citation
876.5820

510(k) Clearances — 1 record

K-Number Device Name Applicant Decision Date Clearance Type Summary
K772355 BLOOD LINE COMP. NEG. PRESS. PILLOW Cordis Corp. 1978-01-26 Traditional PDF ↗

Product code FIW · Class II · Gastroenterology, Urology. Data: openFDA.