Parallax Medical, Inc.
Parallax Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2003.
Top product codes for Parallax Medical, Inc.
Recent clearances by Parallax Medical, Inc.
- K033230 — TRACERS TA BONE CEMENT OPACIFIER, MODEL TCR-TA
- K023445 — TRACERS BONE CEMENT OPACIFIER
- K022169 — CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES
- K011206 — PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES
- K994022 — PARALLAX CRANIOSET
- K991893 — PARALLAX TRACER RADIOPAQUE PARTICLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.