510(k) K863434

THE FIAX 5000 FLUOROMETER by Whittaker Bioproducts, Inc. — Product Code JZT

K863434 is an FDA 510(k) premarket notification submitted by Whittaker Bioproducts, Inc. for the device "THE FIAX 5000 FLUOROMETER". The FDA issued a decision of Substantially Equivalent on October 29, 1986. The device falls under product code JZT (Fluorometer), a Class I device regulated under 21 CFR 866.4520. Whittaker Bioproducts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

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

Device Classification

Device Name
Fluorometer
Device Class
Class I
Regulation Number
866.4520
Review Panel
IM
Submission Type