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FDA 510(k)

DEEG-LITE

K-Number: K972202 · 1997-07-23

ApplicantGrass-Telefactor Product Group
Decision Date1997-07-23
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DEEG-LITE is the device name listed in this FDA 510(k) record. The listed applicant is Grass-Telefactor Product Group. It received FDA 510(k) clearance on 1997-07-23 under 510(k) number K972202. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEEG-LITE?

DEEG-LITE is a medical device that received FDA 510(k) clearance on 1997-07-23. The listed applicant is Grass-Telefactor Product Group. The 510(k) number is K972202.

When did DEEG-LITE receive FDA 510(k) clearance?

DEEG-LITE received FDA 510(k) clearance on 1997-07-23, under 510(k) number K972202.

Who is the listed applicant for DEEG-LITE?

The FDA 510(k) record lists Grass-Telefactor Product Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEEG-LITE?

The FDA product code for DEEG-LITE is GWQ.

Other records listing Grass-Telefactor Product Group 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.

K992291H20- TETHERED OPTIONK974583DEEGLITEK974587H2OK925838TELEFACTOR D/EEG-32K884937BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDINGK870432A1-A2 AMBULATORY EEG CASSETTE RECORDER

View all 12 devices →

Related Devices (Code: GWQ)

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.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, 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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