Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K951130
Device Classification Name
System, Ecg Analysis
More FDA Info for this Device
510(K) Number
K951130
Device Name
System, Ecg Analysis
Applicant
MARQUETTE ELECTRONICS, INC.
8200 WEST TOWER AVE.
MILWAUKEE, WI 53223 US
Other 510(k) Applications for this Company
Contact
KRISTIN PABST
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LOS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/13/1995
Decision Date
04/04/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact