510(k) K952252

ADP REAGENT, MODIFIED by Helena Laboratories — Product Code GHR

K952252 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "ADP REAGENT, MODIFIED". The FDA issued a decision of Substantially Equivalent on September 8, 1995. 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
September 8, 1995
Date Received
May 15, 1995
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