510(k) K833919

CENTRICON MICRO-CONCENTRATOR by Amicon, Inc. — Product Code JJH

K833919 is an FDA 510(k) premarket notification submitted by Amicon, Inc. for the device "CENTRICON MICRO-CONCENTRATOR". The FDA issued a decision of Substantially Equivalent on January 30, 1984. The device falls under product code JJH (Clinical Sample Concentrator), a Class I device regulated under 21 CFR 862.2310. Amicon, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 30, 1984
Date Received
November 14, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Clinical Sample Concentrator
Device Class
Class I
Regulation Number
862.2310
Review Panel
CH
Submission Type