Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MAGNES II BIOMAGNETOMETER

K-Number: K941553 · 1996-05-16

Decision Date1996-05-16
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MAGNES II BIOMAGNETOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Biomagnetic Technologies, Inc.. It received FDA 510(k) clearance on 1996-05-16 under 510(k) number K941553. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNES II BIOMAGNETOMETER?

MAGNES II BIOMAGNETOMETER is a medical device that received FDA 510(k) clearance on 1996-05-16. The listed applicant is Biomagnetic Technologies, Inc.. The 510(k) number is K941553.

When did MAGNES II BIOMAGNETOMETER receive FDA 510(k) clearance?

MAGNES II BIOMAGNETOMETER received FDA 510(k) clearance on 1996-05-16, under 510(k) number K941553.

Who is the listed applicant for MAGNES II BIOMAGNETOMETER?

The FDA 510(k) record lists Biomagnetic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNES II BIOMAGNETOMETER?

The FDA product code for MAGNES II BIOMAGNETOMETER is OLX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Biomagnetic Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: OLX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑