MDRWeb Medical Device Register On-line from Canon Communications, LLC

Search for:

510(k) Premarket Notification Database

Device Classification Name:	MONITOR, BLOOD PRESSURE, INDIRECT, SEMI-AUTOMATIC
Regulation Number:	870.1130 [See Other Products with this regulation number]
510(k) Number:	K032492
Device Name:	BLOOD PRESSURE MONITOR, MODEL KP-7000
Applicant:	K-JUMP HEALTH CO., LTD. 555 THIRTEENTH STREET, NW WASHINGTON, DC 20004 1109
Contact:	JONATHAN S KAHAN
Product Code:	DXN [See Other Manufacturers that make this Product]
Date Received:	08-16-2003
Decision Date:	09-09-2003
Decision:	SE
Advisory Committee:	CV
Statement/Summary/Purged Status:	Summary
Type:	Special
Review by Third Party:	N
Expedited Review:	N

Canon Communications medical device and pharmaceutical media network includes:
Qmed Medical Device & Diagnostic Industry Medical Product & Manufacturing News European Medical Device Technology China Medical Device Manufacturer In Vitro Diagnostic Technology	Med Ad News R&D Directions PharmaLive.com Pharmalot.com eKnowledgebase Pharmaceutical & Medical Packaging News Packaging Digest