FDA 510(k) Application Details - K033063

Device Classification Name	Controls For Blood-Gases, (Assayed And Unassayed)   More FDA Info for this Device
510(K) Number	K033063
Device Name	Controls For Blood-Gases, (Assayed And Unassayed)
Applicant	DIAMOND DIAGNOSTICS, INC. 331 FISKE ST. HOLLISTON, MA 01746 US Other 510(k) Applications for this Company
Contact	LINDA M STUNDTNER Other 510(k) Applications for this Contact
Regulation Number	862.1660   More FDA Info for this Regulation Number
Classification Product Code	JJS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2003
Decision Date	12/12/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review