Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K974425
Device Classification Name
System, Test, Human Chorionic Gonadotropin
More FDA Info for this Device
510(K) Number
K974425
Device Name
System, Test, Human Chorionic Gonadotropin
Applicant
PRINCETON BIOMEDITECH CORP.
4242 U.S. RT. 1
MONMOUTH JUNCTION, NJ 08852-1905 US
Other 510(k) Applications for this Company
Contact
JEMO KANG
Other 510(k) Applications for this Contact
Regulation Number
862.1155
More FDA Info for this Regulation Number
Classification Product Code
DHA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/24/1997
Decision Date
12/24/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact