510(k) K953572

ELX800UV by Bio-Tek Instruments, Inc. — Product Code JJQ

K953572 is an FDA 510(k) premarket notification submitted by Bio-Tek Instruments, Inc. for the device "ELX800UV". The FDA issued a decision of Substantially Equivalent on October 19, 1995. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Bio-Tek Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 19, 1995
Date Received
July 31, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class
Class I
Regulation Number
862.2300
Review Panel
CH
Submission Type