510(k) K063398

ESA LEADCARE II LEAD CONTROL by Bionostics, Inc. — Product Code DIF

K063398 is an FDA 510(k) premarket notification submitted by Bionostics, Inc. for the device "ESA LEADCARE II LEAD CONTROL". The FDA issued a decision of Substantially Equivalent on December 5, 2006. The device falls under product code DIF (Drug Mixture Control Materials), a Class I device regulated under 21 CFR 862.3280. Bionostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 2006
Date Received
November 9, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drug Mixture Control Materials
Device Class
Class I
Regulation Number
862.3280
Review Panel
TX
Submission Type