Lunar Corp.
Lunar Corp. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2000.
Top product codes for Lunar Corp.
Recent clearances by Lunar Corp.
- K001812 — PEDIATRIC REFERENCE DATA
- K001756 — LUNAR REPORT GENERATOR II
- K000826 — PRODIGY LATERAL VIEW SOFTWARE
- K983564 — PRODIGY TOTAL BODY SOFTWARE
- K983724 — ORCA-DX BONE DENSITOMETER
- K983262 — FRACTURE RISK ASSESSMENT OPTION FOR PIXI BONE DENSITOMETERS
- K983269 — FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER
- K983271 — FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERS
- K982267 — DPX-RX BONE DENSITOMETER
- K974437 — EXPERT-XL LATERAL SPINE BMD ACQUISITION AND ANALYSIS SOFTWARE
- K972517 — EXPERT-XL ORTHOPEDIC HIP ACQUISITION AND ANALYSIS SOFTWARE
- K965226 — EXPERT-XL TOTAL BODY ACQUISITION AND ANALYSIS SOFTWARE
- K972053 — PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM
- K964307 — EXPANDED REFERENCE VALUES FOR DPX BON DENSITOMETERS
- K970224 — PIXI BONE DENSITOMETER
- K964263 — EXPERT-KL AND HAND ACQUISITION AND ANALYSIS SOFTWARE
- K961007 — EXPERT SPINE MORPHOTIETRY REFERENCE
- K961944 — LUNAR REPORT GENERATOR
- K960907 — ORCA
- K953032 — LUNAR DPX DENSITOMETER
- K935454 — DPX TISSUE QUANTIFICATION OUTPUT
- K950611 — EXPERT MORPHOMERTY SOFTWARD
- K945526 — LUNAR EXPERT
Data sourced from openFDA. This site is unofficial and independent of the FDA.