510(k) K051218

MODIFICATION TO: UNICAP SPECIFIC IGE by Pharmacia Diagnostics AB — Product Code DHB

K051218 is an FDA 510(k) premarket notification submitted by Pharmacia Diagnostics AB for the device "MODIFICATION TO: UNICAP SPECIFIC IGE". The FDA issued a decision of Substantially Equivalent on June 9, 2005. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Pharmacia Diagnostics AB has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 2005
Date Received
May 12, 2005
Clearance Type
Special
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