FDA 510(k) Application Details - K832933

Device Classification Name	Mercury, Atomic Absorption   More FDA Info for this Device
510(K) Number	K832933
Device Name	Mercury, Atomic Absorption
Applicant	JEROME INSTRUMENT CORP. Other 510(k) Applications for this Company
Regulation Number	862.3600   More FDA Info for this Regulation Number
Classification Product Code	DPH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/1983
Decision Date	11/25/1983
Decision	SE - Substantially Equivalent
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review