Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K955564
Device Classification Name
Tube Tracheostomy And Tube Cuff
More FDA Info for this Device
510(K) Number
K955564
Device Name
Tube Tracheostomy And Tube Cuff
Applicant
RUSCH, INC.
TALL PINES PARK
JAFFREY, NH 03452 US
Other 510(k) Applications for this Company
Contact
NEIL R ARMSTRONG
Other 510(k) Applications for this Contact
Regulation Number
868.5800
More FDA Info for this Regulation Number
Classification Product Code
JOH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/06/1995
Decision Date
06/28/1996
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