Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K990384
Device Classification Name
Nebulizer (Direct Patient Interface)
More FDA Info for this Device
510(K) Number
K990384
Device Name
Nebulizer (Direct Patient Interface)
Applicant
PIPER MEDICAL PRODUCTS
4007 SEAPORT BLVD.
WEST SACRAMENTO, CA 95691 US
Other 510(k) Applications for this Company
Contact
SAMUEL DAVID PIPER, PE
Other 510(k) Applications for this Contact
Regulation Number
868.5630
More FDA Info for this Regulation Number
Classification Product Code
CAF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/08/1999
Decision Date
04/26/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact