510(k) K770564

URIC ACID TEST KIT by Mallinckrodt Critical Care — Product Code CDH

K770564 is an FDA 510(k) premarket notification submitted by Mallinckrodt Critical Care for the device "URIC ACID TEST KIT". The FDA issued a decision of Substantially Equivalent on June 3, 1977. The device falls under product code CDH (Acid, Uric, Phosphotungstate Reduction), a Class I device regulated under 21 CFR 862.1775. Mallinckrodt Critical Care has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 1977
Date Received
March 24, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Uric, Phosphotungstate Reduction
Device Class
Class I
Regulation Number
862.1775
Review Panel
CH
Submission Type