Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K963510
Device Classification Name
Mattress, Air Flotation, Alternating Pressure
More FDA Info for this Device
510(K) Number
K963510
Device Name
Mattress, Air Flotation, Alternating Pressure
Applicant
MELLEN AIR MFG., INC.
2840 TEMPLE AVE.
LONG BEACH, CA 90806 US
Other 510(k) Applications for this Company
Contact
BERTRAND H WEIDBERG
Other 510(k) Applications for this Contact
Regulation Number
880.5550
More FDA Info for this Regulation Number
Classification Product Code
FNM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/03/1996
Decision Date
11/26/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact