510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011017Substantially Equivalent

Promax-Xp, TENS and Microcurrent Device; Promax-TENS, TENS Device; Promax-Libra, TENS Device; Promax-Mc, Microcurrent

Rehabilicare, Inc., New Brighton MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K011017 is the FDA 510(k) clearance record for PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT, a class II device, cleared for Rehabilicare, Inc. on under FDA product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief). FDA records list 4 510(k) clearances for Rehabilicare, Inc., from to . As of , FDA records show no recalls naming K011017.

Clearance record

Decision date
Received
(173 days to decision)
Product code
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
Rehabilicare, Inc. 1811 Old Hwy. 8, New Brighton MN
510(k) summary
Summary
Third party review
No

Clearances, product code GZJ

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