510(k) K012723

PLATELETWORKS by Helena Laboratories — Product Code JOZ

K012723 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "PLATELETWORKS". The FDA issued a decision of Substantially Equivalent on September 28, 2001. The device falls under product code JOZ (System, Automated Platelet Aggregation), a Class II device regulated under 21 CFR 864.5700. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 28, 2001
Date Received
August 15, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Automated Platelet Aggregation
Device Class
Class II
Regulation Number
864.5700
Review Panel
HE
Submission Type