510(k) K902266

ELECTROLYTE CONTROLS (ASSAYED AND UNASSAYED) by Phoenix Diagnostics, Inc. — Product Code JJR

K902266 is an FDA 510(k) premarket notification submitted by Phoenix Diagnostics, Inc. for the device "ELECTROLYTE CONTROLS (ASSAYED AND UNASSAYED)". The FDA issued a decision of Substantially Equivalent on June 6, 1990. The device falls under product code JJR (Electrolyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Phoenix Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 1990
Date Received
May 21, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrolyte Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type