Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K990037
Device Classification Name
Apparatus, Exhaust, Surgical
More FDA Info for this Device
510(K) Number
K990037
Device Name
Apparatus, Exhaust, Surgical
Applicant
AMERICAN IMMUNO TECH
320 KALMUS DR.
COSTA MESA, CA 92626 US
Other 510(k) Applications for this Company
Contact
ESTHER SALTZ
Other 510(k) Applications for this Contact
Regulation Number
878.5070
More FDA Info for this Regulation Number
Classification Product Code
FYD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/06/1999
Decision Date
08/24/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact