Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K001742
Device Classification Name
Valve, Non-Rebreathing
More FDA Info for this Device
510(K) Number
K001742
Device Name
Valve, Non-Rebreathing
Applicant
LAERDAL MEDICAL CORP.
49 PLAIN ST.
NORTH ATTLEBORO, MA 02760 US
Other 510(k) Applications for this Company
Contact
CYNTHIA J NOLTE
Other 510(k) Applications for this Contact
Regulation Number
868.5870
More FDA Info for this Regulation Number
Classification Product Code
CBP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/08/2000
Decision Date
10/06/2000
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