510(k) K910800

ADP REAGENT by Helena Laboratories — Product Code GHR

K910800 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "ADP REAGENT". The FDA issued a decision of Substantially Equivalent on May 20, 1991. The device falls under product code GHR (Reagent, 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
May 20, 1991
Date Received
February 25, 1991
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