510(k) K001344

ADVIA IMS by Bayer Corp. — Product Code DIH

K001344 is an FDA 510(k) premarket notification submitted by Bayer Corp. for the device "ADVIA IMS". The FDA issued a decision of Substantially Equivalent on June 26, 2000. The device falls under product code DIH (Colorimetry, Cholinesterase), a Class I device regulated under 21 CFR 862.3240. Bayer Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 26, 2000
Date Received
April 27, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimetry, Cholinesterase
Device Class
Class I
Regulation Number
862.3240
Review Panel
TX
Submission Type