510(k) K871838

BIOMEK 1000C AUTOMATED LABORATORY WORK STATION by Beckman Instruments, Inc. — Product Code JJG

K871838 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "BIOMEK 1000C AUTOMATED LABORATORY WORK STATION". The FDA issued a decision of Substantially Equivalent on May 26, 1987. The device falls under product code JJG (Analyzer, Chemistry, Centrifugal, For Clinical Use), a Class I device regulated under 21 CFR 862.2140. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 26, 1987
Date Received
May 12, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Chemistry, Centrifugal, For Clinical Use
Device Class
Class I
Regulation Number
862.2140
Review Panel
CH
Submission Type