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FDA 510(k)

MAGNES 2500 WH BIOMAGNETOMETER

K-Number: K962317 · 1997-05-07

Decision Date1997-05-07
Product CodeOLY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MAGNES 2500 WH 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 1997-05-07 under 510(k) number K962317. The device is classified under product code OLY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNES 2500 WH BIOMAGNETOMETER?

MAGNES 2500 WH BIOMAGNETOMETER is a medical device that received FDA 510(k) clearance on 1997-05-07. The listed applicant is Biomagnetic Technologies, Inc.. The 510(k) number is K962317.

When did MAGNES 2500 WH BIOMAGNETOMETER receive FDA 510(k) clearance?

MAGNES 2500 WH BIOMAGNETOMETER received FDA 510(k) clearance on 1997-05-07, under 510(k) number K962317.

Who is the listed applicant for MAGNES 2500 WH 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 2500 WH BIOMAGNETOMETER?

The FDA product code for MAGNES 2500 WH BIOMAGNETOMETER is OLY.

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: OLY)

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

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

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