510(k) K843893

MAGNESIUM REAGENT SET by Livonia Diagnostics, Inc. — Product Code JGJ

K843893 is an FDA 510(k) premarket notification submitted by Livonia Diagnostics, Inc. for the device "MAGNESIUM REAGENT SET". The FDA issued a decision of Substantially Equivalent on October 30, 1984. The device falls under product code JGJ (Photometric Method, Magnesium), a Class I device regulated under 21 CFR 862.1495. Livonia Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 1984
Date Received
October 3, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Photometric Method, Magnesium
Device Class
Class I
Regulation Number
862.1495
Review Panel
CH
Submission Type