510(k) K781572

NORMAL HEMATOLOGY CONTROL UNASSAYED by Ortho Diagnostics, Inc. — Product Code JPK

K781572 is an FDA 510(k) premarket notification submitted by Ortho Diagnostics, Inc. for the device "NORMAL HEMATOLOGY CONTROL UNASSAYED". The FDA issued a decision of Substantially Equivalent on October 17, 1978. The device falls under product code JPK (Mixture, Hematology Quality Control), a Class II device regulated under 21 CFR 864.8625. Ortho Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 17, 1978
Date Received
September 14, 1978
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