510(k) K121981

ADVIA CENTAUR INACT PARATHYROID HORMONE (IPTH) ASSAY by Siemens Healthcare Diagnostics — Product Code CEW

K121981 is an FDA 510(k) premarket notification submitted by Siemens Healthcare Diagnostics for the device "ADVIA CENTAUR INACT PARATHYROID HORMONE (IPTH) ASSAY". The FDA issued a decision of Substantially Equivalent on March 21, 2013. The device falls under product code CEW (Radioimmunoassay, Parathyroid Hormone), a Class II device regulated under 21 CFR 862.1545. Siemens Healthcare Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 21, 2013
Date Received
July 6, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Parathyroid Hormone
Device Class
Class II
Regulation Number
862.1545
Review Panel
CH
Submission Type