510(k) K010598

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL by Quantimetrix Corp. — Product Code JPK

K010598 is an FDA 510(k) premarket notification submitted by Quantimetrix Corp. for the device "SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL". The FDA issued a decision of Substantially Equivalent on March 23, 2001. The device falls under product code JPK (Mixture, Hematology Quality Control), a Class II device regulated under 21 CFR 864.8625. Quantimetrix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 2001
Date Received
February 28, 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