510(k) K801481

BMC RIAFLO SYSTEM by Boehringer Mannheim Corp. — Product Code JJC

K801481 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "BMC RIAFLO SYSTEM". The FDA issued a decision of Substantially Equivalent on August 20, 1980. The device falls under product code JJC (Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use), a Class I device regulated under 21 CFR 862.2150. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 20, 1980
Date Received
June 24, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use
Device Class
Class I
Regulation Number
862.2150
Review Panel
CH
Submission Type