510(k) K865057

TANDEMR ICONR II HCG(SERUM) IMMUNOENZYMETRIC ASSAY by Hybritech, Inc. — Product Code JHI

K865057 is an FDA 510(k) premarket notification submitted by Hybritech, Inc. for the device "TANDEMR ICONR II HCG(SERUM) IMMUNOENZYMETRIC ASSAY". The FDA issued a decision of Substantially Equivalent on March 10, 1987. The device falls under product code JHI (Visual, Pregnancy Hcg, Prescription Use), a Class II device regulated under 21 CFR 862.1155. Hybritech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 1987
Date Received
December 24, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Visual, Pregnancy Hcg, Prescription Use
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type