MENTOR 150 TRANSCUTANEOUS NERVE STIMULA— 510(k) K803121

Name: FDA 510(k) clearance K803121
Creator: U.S. Food and Drug Administration
Published: 1980-12-30

Substantially Equivalent

George H. Frisch

FDA 510(k) clearance K803121 for MENTOR 150 TRANSCUTANEOUS NERVE STIMULA, Substantially Equivalent on 1980-12-30. Applicant: George H. Frisch. Device class: 2.

Clearance details

Applicant: George H. Frisch
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1980-12-11
Decision date: 1980-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZJ

view all

K252712 — STIMPOD NMS460 Nerve Stimulator2026-05-28
K252767 — actiTENS mini2026-01-16
K252236 — CP Relief Wand Rx - TENS/NMES2025-08-15
K232441 — Unipro (K-UNIPRO-US)2024-08-30
K241228 — TENSWave2024-08-27

More clearances from George H. Frisch

view all

K803113 — MENTOR 402 TRANSCUTANEOUS ELEC. STIMULAT1980-12-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.