Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K984031
Device Classification Name
Spirometer, Diagnostic
More FDA Info for this Device
510(K) Number
K984031
Device Name
Spirometer, Diagnostic
Applicant
SCHILLER AG
ALTGASSE 68
BAAR CH-6341 CH
Other 510(k) Applications for this Company
Contact
MARKUS BUETLER
Other 510(k) Applications for this Contact
Regulation Number
868.1840
More FDA Info for this Regulation Number
Classification Product Code
BZG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/12/1998
Decision Date
04/30/1999
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