LAURUS NEEDLE CORE BIOPSY SYSTEM — Laurus Medical Corp. (510(k) K960317)

Name: LAURUS NEEDLE CORE BIOPSY SYSTEM — Laurus Medical Corp. (510(k) K960317)
Creator: DeviceClear

LAURUS NEEDLE CORE BIOPSY SYSTEM — Laurus Medical Corp. (510(k) K960317) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: LAURUS NEEDLE CORE BIOPSY SYSTEM; Applicant: Laurus Medical Corp.; Clearance track: 510(k).

Device name	LAURUS NEEDLE CORE BIOPSY SYSTEM
Applicant	Laurus Medical Corp.
Clearance track	510(k)
Submission number	K960317
Decision	Substantially Equivalent
Decision date	1996-03-15
Date received	1996-01-23
Product code	FCG
Device class	2
Medical specialty	Gastroenterology, Urology
Applicant location	CA, US
Source	openFDA device

🔍 Search all device clearances →

$1999/mo

Try DeviceClear →