510(k) K020532

POLYMEDCO HBA1C TEST by Polymedco, Inc. — Product Code LCP

K020532 is an FDA 510(k) premarket notification submitted by Polymedco, Inc. for the device "POLYMEDCO HBA1C TEST". The FDA issued a decision of Substantially Equivalent on April 24, 2002. The device falls under product code LCP (Assay, Glycosylated Hemoglobin), a Class II device regulated under 21 CFR 864.7470. Polymedco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 24, 2002
Date Received
February 19, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Assay, Glycosylated Hemoglobin
Device Class
Class II
Regulation Number
864.7470
Review Panel
HE
Submission Type