510(k) K862175

WHITE OAK ALLERGEN DISC by Immuno Nuclear Corp. — Product Code DHB

K862175 is an FDA 510(k) premarket notification submitted by Immuno Nuclear Corp. for the device "WHITE OAK ALLERGEN DISC". The FDA issued a decision of Substantially Equivalent on June 20, 1986. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Immuno Nuclear Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1986
Date Received
June 9, 1986
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