510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020364Substantially Equivalent

Phoenix Ise Reagents for Beckman Cx Systems

Phoenix Diagnostics, Inc., Natick MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K020364 is the FDA 510(k) clearance record for PHOENIX ISE REAGENTS FOR BECKMAN CX SYSTEMS, a class II device, cleared for Phoenix Diagnostics, Inc. on under FDA product code JGS (Electrode, Ion Specific, Sodium). FDA records list 21 510(k) clearances for Phoenix Diagnostics, Inc., from to . As of , FDA records show no recalls naming K020364.

Clearance record

Decision date
Received
(120 days to decision)
Product code
JGS Electrode, Ion Specific, Sodium
Regulation
21 CFR 862.1665
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Phoenix Diagnostics, Inc. 8 Tech Cir., Natick MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JGS

Trailing 12 months
1 clearance under product code JGS in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JGS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260