Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K102567
Device Classification Name
Ventilatory Effort Recorder
More FDA Info for this Device
510(K) Number
K102567
Device Name
Ventilatory Effort Recorder
Applicant
ITAMAR MEDICAL LTD
555 THIRTEENTH STREET, NW
WASHINGTON, DC 20004-1109 US
Other 510(k) Applications for this Company
Contact
JONATHAN KAHN
Other 510(k) Applications for this Contact
Regulation Number
868.2375
More FDA Info for this Regulation Number
Classification Product Code
MNR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/07/2010
Decision Date
06/02/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact