510(k) K113841

IMMUNOCAP ALLERGEN COMPONENTS BUNDLE by Phadia US, Inc. — Product Code DHB

K113841 is an FDA 510(k) premarket notification submitted by Phadia US, Inc. for the device "IMMUNOCAP ALLERGEN COMPONENTS BUNDLE". The FDA issued a decision of Substantially Equivalent on September 13, 2012. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Phadia US, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 13, 2012
Date Received
December 28, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Radioallergosorbent (Rast) Immunological
Device Class
Class II
Regulation Number
866.5750
Review Panel
IM
Submission Type