FDA 510(k)

700 SERIES BIOMAGNETOMETER

K-Number: K901215 · 1990-06-25

Decision Date1990-06-25

Product CodeOLX

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

700 SERIES 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 1990-06-25 under 510(k) number K901215. 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 700 SERIES BIOMAGNETOMETER?

700 SERIES BIOMAGNETOMETER is a medical device that received FDA 510(k) clearance on 1990-06-25. The listed applicant is Biomagnetic Technologies, Inc.. The 510(k) number is K901215.

When did 700 SERIES BIOMAGNETOMETER receive FDA 510(k) clearance?

700 SERIES BIOMAGNETOMETER received FDA 510(k) clearance on 1990-06-25, under 510(k) number K901215.

Who is the listed applicant for 700 SERIES 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 700 SERIES BIOMAGNETOMETER?

The FDA product code for 700 SERIES BIOMAGNETOMETER is OLX.

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Other records listing Biomagnetic Technologies, Inc. as applicant

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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.