510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962317Substantially Equivalent

Magnes 2500 Wh Biomagnetometer

Biomagnetic Technologies, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962317 is the FDA 510(k) clearance record for MAGNES 2500 WH BIOMAGNETOMETER, a class II device, cleared for Biomagnetic Technologies, Inc. on under FDA product code OLY (Magnetoencephalograph). FDA's definition for product code OLY reads: "Acquire, display, store, and archive biomagnetic signals produced by electrically active nerve tissue in the brain to provide information about the location of active nerve tissue responsible for certain brain functions relative to brain...". FDA records list 8 510(k) clearances for Biomagnetic Technologies, Inc., from to . As of , FDA records show no recalls naming K962317.

Clearance record

Decision date
Received
(324 days to decision)
Product code
OLY Magnetoencephalograph
Regulation
21 CFR 882.1400
Device class
Class II
Review panel
Neurology
Applicant
Biomagnetic Technologies, Inc. 9727 Pacific Heights Blvd., San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code OLY

Trailing 12 months

FDA records hold no clearances under product code OLY in the trailing twelve months.

FDA records show no clearances under product code OLY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OLY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260