BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEG— 510(k) K993708

Name: FDA 510(k) clearance K993708
Creator: U.S. Food and Drug Administration
Published: 1999-12-03

Substantially Equivalent

Biomagnetic Technologies, Inc.

FDA 510(k) clearance K993708 for BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEG, Substantially Equivalent on 1999-12-03. Applicant: Biomagnetic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Biomagnetic Technologies, Inc.
Product code: Code OLX
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1999-11-03
Decision date: 1999-12-03
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OLX

view all

K260563 — CN-Suite2026-08-16
K252565 — PreOp v32026-02-13
K250239 — NeuroMatch2025-05-23
K241513 — Sourcerer2024-09-27
K233985 — TRIUX neo (NM27000N ); MEGreview (SW26241N-B)2024-05-15

More clearances from Biomagnetic Technologies, Inc.

view all

K962317 — MAGNES 2500 WH BIOMAGNETOMETER1997-05-07
K941553 — MAGNES II BIOMAGNETOMETER1996-05-16
K921821 — IBT MODEL SVI1992-11-02
K913604 — SOMATOSENSORY STIMULUS SYSTEM1991-12-09
K901215 — 700 SERIES BIOMAGNETOMETER1990-06-25

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