510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023050Substantially Equivalent

Reliant Btl 5000 Puls Electrical Stimulation System, Reliant Btl 5000 Sono Ultrasound System, Reliant Btl 5000 Combi

Reliant Technologies, Inc., Angels Camp CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023050 is the FDA 510(k) clearance record for RELIANT BTL 5000 PULS ELECTRICAL STIMULATION SYSTEM, RELIANT BTL 5000 SONO ULTRASOUND SYSTEM, RELIANT BTL 5000 COMBI, a class II device, cleared for Reliant Technologies, Inc. on under FDA product code IMG (Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat). FDA records list 19 510(k) clearances for Reliant Technologies, Inc., from to . As of , FDA records show no recalls naming K023050.

Clearance record

Decision date
Received
(154 days to decision)
Product code
IMG Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
Regulation
21 CFR 890.5860
Device class
Class II
Review panel
Physical Medicine
Applicant
Reliant Technologies, Inc. P.O. Box 405, Angels Camp CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IMG

Trailing 12 months

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

FDA records show no clearances under product code IMG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IMG, 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