Device Classification Name |
Apparatus, Suction, Ward Use, Portable, Ac-Powered
More FDA Info for this Device |
510(K) Number |
K011725 |
Device Name |
Apparatus, Suction, Ward Use, Portable, Ac-Powered |
Applicant |
KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT), LTD.
STOCK RD.
SOUTHEND-ON-SEA, ESSEX SS25QH GB
Other 510(k) Applications for this Company
|
Contact |
ROGER GRAY
Other 510(k) Applications for this Contact |
Regulation Number |
878.4780
More FDA Info for this Regulation Number |
Classification Product Code |
JCX
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
06/04/2001 |
Decision Date |
08/31/2001 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
SU - General & Plastic Surgery |
Review Advisory Committee |
SU - General & Plastic Surgery |
Statement / Summary / Purged Status |
Statement |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|