510(k) K821872

ULTRACHEM URIC ACID AIDH by Harleco Diagnostics — Product Code CDO

K821872 is an FDA 510(k) premarket notification submitted by Harleco Diagnostics for the device "ULTRACHEM URIC ACID AIDH". The FDA issued a decision of Substantially Equivalent on July 14, 1982. The device falls under product code CDO (Acid, Uric, Uricase (U.V.)), a Class I device regulated under 21 CFR 862.1775. Harleco Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 14, 1982
Date Received
June 25, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Uric, Uricase (U.V.)
Device Class
Class I
Regulation Number
862.1775
Review Panel
CH
Submission Type