Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K141582
Device Classification Name
Electrocardiograph
More FDA Info for this Device
510(K) Number
K141582
Device Name
Electrocardiograph
Applicant
WELCH ALLYN
4341 STATE STREET ROAD
SKANEATELES FALLS, NY 13153 US
Other 510(k) Applications for this Company
Contact
KEVIN CROSSEN
Other 510(k) Applications for this Contact
Regulation Number
870.2340
More FDA Info for this Regulation Number
Classification Product Code
DPS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/13/2014
Decision Date
07/11/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact