510(k) K960592

ELECTROLYTE STANDARDS by Phoenix Diagnostics, Inc. — Product Code JJR

K960592 is an FDA 510(k) premarket notification submitted by Phoenix Diagnostics, Inc. for the device "ELECTROLYTE STANDARDS". The FDA issued a decision of Substantially Equivalent on May 13, 1996. 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
May 13, 1996
Date Received
February 12, 1996
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