510(k) K023544

GENZYME CONTRAST II HCG URINE/SERUM TEST by Genzyme Corp. — Product Code JHI

K023544 is an FDA 510(k) premarket notification submitted by Genzyme Corp. for the device "GENZYME CONTRAST II HCG URINE/SERUM TEST". The FDA issued a decision of Substantially Equivalent on January 16, 2003. The device falls under product code JHI (Visual, Pregnancy Hcg, Prescription Use), a Class II device regulated under 21 CFR 862.1155. Genzyme Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 16, 2003
Date Received
October 22, 2002
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