510(k) K941110

PARAKIT by Hardy Diagnostics — Product Code LKS

K941110 is an FDA 510(k) premarket notification submitted by Hardy Diagnostics for the device "PARAKIT". The FDA issued a decision of Substantially Equivalent on May 17, 1994. The device falls under product code LKS (Device, Parasite Concentration), a Class I device regulated under 21 CFR 866.2900. Hardy Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 17, 1994
Date Received
March 7, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Parasite Concentration
Device Class
Class I
Regulation Number
866.2900
Review Panel
MI
Submission Type