510(k) K862148

OLYMPUS AU 5000 FLAME PHOTOMETER MODULE by Olympus Corp. — Product Code JJO

K862148 is an FDA 510(k) premarket notification submitted by Olympus Corp. for the device "OLYMPUS AU 5000 FLAME PHOTOMETER MODULE". The FDA issued a decision of Substantially Equivalent on September 29, 1986. The device falls under product code JJO (Flame Emission Photometer For Clinical Use), a Class I device regulated under 21 CFR 862.2540. Olympus Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 29, 1986
Date Received
June 4, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Flame Emission Photometer For Clinical Use
Device Class
Class I
Regulation Number
862.2540
Review Panel
CH
Submission Type