Leiker Regulatory & Quality Consulting

Leiker Regulatory & Quality Consulting holds 1 FDA 510(k) medical device clearance, cleared in 2012.

Top product codes for Leiker Regulatory & Quality Consulting

IYO — Radiology1 device

Recent clearances by Leiker Regulatory & Quality Consulting

K112539 — CHISON DIGITAL ULTRASOUND SYSTEM, CONVEX PROBE, LINEAR PROBE, TRANSVAGINAL MICRO-CONVEX PROBE, TRANSRECTAL LINEAR PROBECode IYO·2012-01-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.