FDA 510(k), K990519, PHOENIX EPIDURAL & SPINAL NEEDLES

510(K) Number: K990519
Device Name: PHOENIX EPIDURAL & SPINAL NEEDLES
Manufacturer: MYCO MEDICAL SUPPLIES, INC.
Device Classification Name: Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation Number: 868.5150
Classification Product Code: BSP
Date Received: 02/18/1999
Decision Date: 06/02/2000
Regulation Medical Specialty: Anesthesiology

120 pages (76 of 196 pages are fully redacted)