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FDA 510(k)

NEUROMAG-122

K-Number: K962764 · 1996-10-31

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1996-10-31
Product CodeOLY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMAG-122 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1996-10-31 under 510(k) number K962764. 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 NEUROMAG-122?

NEUROMAG-122 is a medical device that received FDA 510(k) clearance on 1996-10-31. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K962764.

When did NEUROMAG-122 receive FDA 510(k) clearance?

NEUROMAG-122 received FDA 510(k) clearance on 1996-10-31, under 510(k) number K962764.

Who is the listed applicant for NEUROMAG-122?

The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROMAG-122?

The FDA product code for NEUROMAG-122 is OLY.

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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.

K191785Orion LifeSpan MEGCompumedics LimitedK152184MagView BIOMAGNETOMETER SYSTEMTristan Technologies, Inc.K962317MAGNES 2500 WH BIOMAGNETOMETERBiomagnetic Technologies, Inc.K854466BIOMAGNETIC TECHNOLOGIES NEUROMAGNEOMETERBiomagnetic Technologies, Inc.

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.

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