Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K961074
Device Classification Name
Light, Surgical, Floor Standing
More FDA Info for this Device
510(K) Number
K961074
Device Name
Light, Surgical, Floor Standing
Applicant
CUDA PRODUCTS CO.
6000 POWERS AVE.
JACKSONVILLE, FL 32217 US
Other 510(k) Applications for this Company
Contact
KIM REED
Other 510(k) Applications for this Contact
Regulation Number
878.4580
More FDA Info for this Regulation Number
Classification Product Code
FSS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/18/1996
Decision Date
04/30/1996
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact