LISS CRANIAL STIMULATOR MODEL SBL201-M— 510(k) K894515

Name: FDA 510(k) clearance K894515
Creator: U.S. Food and Drug Administration
Published: 1990-05-03

Substantially Equivalent

Medical Consultants Intl. , Ltd.

FDA 510(k) clearance K894515 for LISS CRANIAL STIMULATOR MODEL SBL201-M, Substantially Equivalent on 1990-05-03. Applicant: Medical Consultants Intl. , Ltd.. Device class: 2.

Clearance details

Applicant: Medical Consultants Intl. , Ltd.
Product code: Code QJQ
Device class: Class 2
Regulation: 21 CFR 882.5800
Advisory panel: Neurology
Date received: 1989-07-19
Decision date: 1990-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Rock, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QJQ

view all

K252951 — Genesis Sleep2025-12-31
K232253 — Modius Stress2024-03-27
K230826 — Modius Sleep2023-10-27
K182311 — Cervella2019-03-07
K090052 — CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/C2009-05-29

More clearances from Medical Consultants Intl. , Ltd.

view all

K904264 — MODEL SW-103 SOLITANS STIMULATOR1991-05-09
K900731 — MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)1990-12-17
K903654 — LISS CRANIAL STIMULATOR MODEL SBL202-B1990-10-04
K902976 — MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC1990-09-07
K896226 — LISS BODY STIMULATOR MODEL SBL501-M1990-04-10

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