Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K951222
Device Classification Name
Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)
More FDA Info for this Device
510(K) Number
K951222
Device Name
Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)
Applicant
RANDOX LABORATORIES, LTD.
ARDMORE, DIAMOND ROAD
CRUMLIN BT29 4QY IE
Other 510(k) Applications for this Company
Contact
John Lamont
Other 510(k) Applications for this Contact
Regulation Number
862.1645
More FDA Info for this Regulation Number
Classification Product Code
JIR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/20/1995
Decision Date
04/24/1996
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