510(k) K922800

PLATELET AGGREGATION REAGENTS by Chrono-Log Corp. — Product Code GHR

K922800 is an FDA 510(k) premarket notification submitted by Chrono-Log Corp. for the device "PLATELET AGGREGATION REAGENTS". The FDA issued a decision of Substantially Equivalent on August 26, 1992. The device falls under product code GHR (Reagent, Platelet Aggregation), a Class II device regulated under 21 CFR 864.5700. Chrono-Log Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 26, 1992
Date Received
June 10, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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