510(k) K862174

TIMOTHY ALLERGEN DISC by Immuno Nuclear Corp. — Product Code DGC

K862174 is an FDA 510(k) premarket notification submitted by Immuno Nuclear Corp. for the device "TIMOTHY ALLERGEN DISC". The FDA issued a decision of Substantially Equivalent on August 6, 1986. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Immuno Nuclear Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 6, 1986
Date Received
June 9, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ige, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type