510(k) K915825

MARATHON 6K GENERAL-PURPOSE CENTRIFUGE by Fisher Scientific Co., LLC — Product Code GKF

K915825 is an FDA 510(k) premarket notification submitted by Fisher Scientific Co., LLC for the device "MARATHON 6K GENERAL-PURPOSE CENTRIFUGE". The FDA issued a decision of Substantially Equivalent on March 11, 1992. The device falls under product code GKF (Instrument, Hematocrit, Automated), a Class II device regulated under 21 CFR 864.5600. Fisher Scientific Co., LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 1992
Date Received
December 30, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Hematocrit, Automated
Device Class
Class II
Regulation Number
864.5600
Review Panel
HE
Submission Type