510(k) K823558

MICRO-HEMATOCRIT CENTRIFUGE 335/336 by Fisher Scientific Co., LLC — Product Code JPI

K823558 is an FDA 510(k) premarket notification submitted by Fisher Scientific Co., LLC for the device "MICRO-HEMATOCRIT CENTRIFUGE 335/336". The FDA issued a decision of Substantially Equivalent on January 21, 1983. The device falls under product code JPI (Device, Hematocrit Measuring), a Class II device regulated under 21 CFR 864.6400. Fisher Scientific Co., LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 1983
Date Received
December 2, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Hematocrit Measuring
Device Class
Class II
Regulation Number
864.6400
Review Panel
HE
Submission Type