510(k) K013898

R&D RET-LINE KIT by R&D Systems, Inc. — Product Code JPK

K013898 is an FDA 510(k) premarket notification submitted by R&D Systems, Inc. for the device "R&D RET-LINE KIT". The FDA issued a decision of Substantially Equivalent on January 22, 2002. The device falls under product code JPK (Mixture, Hematology Quality Control), a Class II device regulated under 21 CFR 864.8625. R&D Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 2002
Date Received
November 23, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mixture, Hematology Quality Control
Device Class
Class II
Regulation Number
864.8625
Review Panel
HE
Submission Type