510(k) K933548

ELS 1000 by Bio-Tek Instruments, Inc. — Product Code JJE

K933548 is an FDA 510(k) premarket notification submitted by Bio-Tek Instruments, Inc. for the device "ELS 1000". The FDA issued a decision of Substantially Equivalent on October 29, 1993. The device falls under product code JJE (Analyzer, Chemistry (Photometric, Discrete), For Clinical Use), a Class I device regulated under 21 CFR 862.2160. Bio-Tek Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 29, 1993
Date Received
July 20, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
Device Class
Class I
Regulation Number
862.2160
Review Panel
CH
Submission Type