510(k) K260331

IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13) by Siemens Healthcare Diagnostics Products, Ltd. — Product Code DHB

K260331 is an FDA 510(k) premarket notification submitted by Siemens Healthcare Diagnostics Products, Ltd. for the device "IMMULITE 2000 3gAllergy Specific IgE Vantage; IMMULITE 2000 Systems Peanut Allergen (F13)". The FDA issued a decision of Substantially Equivalent on September 4, 2026. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Siemens Healthcare Diagnostics Products, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 4, 2026
Date Received
February 2, 2026
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