510(k) K893768

MODIFIED PK300 AUTOMATIC EIA ANALYZER by Olympus Corp. — Product Code JJF

K893768 is an FDA 510(k) premarket notification submitted by Olympus Corp. for the device "MODIFIED PK300 AUTOMATIC EIA ANALYZER". The FDA issued a decision of Substantially Equivalent on August 15, 1989. The device falls under product code JJF (Analyzer, Chemistry, Micro, For Clinical Use), a Class I device regulated under 21 CFR 862.2170. Olympus Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 1989
Date Received
May 19, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Chemistry, Micro, For Clinical Use
Device Class
Class I
Regulation Number
862.2170
Review Panel
CH
Submission Type