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FDA Product Code

FDA Product Code HDL — Clearance Directory

Device Class
Class I
21 CFR Citation
884.4520

510(k) Clearances — 2 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K891038 VAGINAL RETRACTORS - KRISTELLER, DELEE, BREISKY Zinnanti Surgical Instruments, Inc. 1989-03-17 Traditional PDF ↗
K780349 VAGINAL RETRACTOR Edward Weck, Inc. 1978-03-14 Traditional PDF ↗

Product code HDL · Class I · Obstetrics/Gynecology. Data: openFDA.