Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K024339
Device Classification Name
Cholinesterase Test Paper
More FDA Info for this Device
510(K) Number
K024339
Device Name
Cholinesterase Test Paper
Applicant
COZART BIOSCIENCE LTD.
45 MILTON PARK
ABINGDON
OXFORDSHIRE OX14 4RU OX14 4RU GB
Other 510(k) Applications for this Company
Contact
ROBERTO LIDDI
Other 510(k) Applications for this Contact
Regulation Number
862.3240
More FDA Info for this Regulation Number
Classification Product Code
DIG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/27/2002
Decision Date
04/07/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
TX - Clinical Toxicology
Review Advisory Committee
TX - Clinical Toxicology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact