MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)— 510(k) K900731

Name: FDA 510(k) clearance K900731
Creator: U.S. Food and Drug Administration
Published: 1990-12-17

Substantially Equivalent

Medical Consultants Intl. , Ltd.

FDA 510(k) clearance K900731 for MEDI LISS DENTAL ANALGESIA DEVICE (SBL601), Substantially Equivalent on 1990-12-17. Applicant: Medical Consultants Intl. , Ltd.. Device class: Unclassified.

Clearance details

Applicant: Medical Consultants Intl. , Ltd.
Product code: Product code LWM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1990-02-15
Decision date: 1990-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Rock, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LWM

view all

K193570 — Dental Pain Eraser2020-01-17
K192429 — Dental Pain Eraser2020-01-14
K182947 — Dental Pain Eraser2019-03-26
K011001 — TEAM-UP TM DENTAL ELECTRONIC ANESTHESIA SYSTEM2001-06-07
K935304 — 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 86701994-03-16

More clearances from Medical Consultants Intl. , Ltd.

view all

K904264 — MODEL SW-103 SOLITANS STIMULATOR1991-05-09
K903654 — LISS CRANIAL STIMULATOR MODEL SBL202-B1990-10-04
K902976 — MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC1990-09-07
K894515 — LISS CRANIAL STIMULATOR MODEL SBL201-M1990-05-03
K896226 — LISS BODY STIMULATOR MODEL SBL501-M1990-04-10

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