510(k) K932662

CYCLOSPORINE (WHOLE BLOOD) CONTROL-PEDIATRIC LEVEL by More Diagnostics — Product Code LAS

K932662 is an FDA 510(k) premarket notification submitted by More Diagnostics for the device "CYCLOSPORINE (WHOLE BLOOD) CONTROL-PEDIATRIC LEVEL". The FDA issued a decision of Substantially Equivalent on July 26, 1993. The device falls under product code LAS (Drug Specific Control Materials), a Class I device regulated under 21 CFR 862.3280. More Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 26, 1993
Date Received
June 2, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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