510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K850508Substantially Equivalent

Logikal Lontophoresis Unit -Anesthesia Inotophores

Kal Life Systems, Mission Viejo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850508 is the FDA 510(k) clearance record for LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES, a class II device, cleared for Kal Life Systems on under FDA product code EGJ (Device, Iontophoresis, Other Uses). FDA records list one 510(k) clearance for Kal Life Systems. As of , FDA records show no recalls naming K850508.

Clearance record

Decision date
Received
(96 days to decision)
Product code
EGJ Device, Iontophoresis, Other Uses
Regulation
21 CFR 890.5525
Device class
Class II
Review panel
Physical Medicine
Applicant
Kal Life Systems 24581 Saturna, Mission Viejo CA
Third party review
No

Clearances, product code EGJ

Trailing 12 months

FDA records hold no clearances under product code EGJ in the trailing twelve months.

FDA records show no clearances under product code EGJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EGJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260