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FDA 510(k) Application Details - K051110
Device Classification Name
System, Test, Vitamin D
More FDA Info for this Device
510(K) Number
K051110
Device Name
System, Test, Vitamin D
Applicant
IMMUNODIAGNOSTIC SYSTEMS LTD.
10 DIDCOT WAY,
BOLDEN BUSINESS PARK
BOLDON, TYNE & WEAR NE35 9PD GB
Other 510(k) Applications for this Company
Contact
PAUL PUNTIN
Other 510(k) Applications for this Contact
Regulation Number
862.1825
More FDA Info for this Regulation Number
Classification Product Code
MRG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/02/2005
Decision Date
07/06/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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