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FDA 510(k)

STD-228 SPECTRAL TREND DISPLAY

K-Number: K871480 · 1987-05-01

ApplicantGrass-Telefactor Product Group
Decision Date1987-05-01
Product CodeGWS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STD-228 SPECTRAL TREND DISPLAY 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 1987-05-01 under 510(k) number K871480. The device is classified under product code GWS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STD-228 SPECTRAL TREND DISPLAY?

STD-228 SPECTRAL TREND DISPLAY is a medical device that received FDA 510(k) clearance on 1987-05-01. The listed applicant is Grass-Telefactor Product Group. The 510(k) number is K871480.

When did STD-228 SPECTRAL TREND DISPLAY receive FDA 510(k) clearance?

STD-228 SPECTRAL TREND DISPLAY received FDA 510(k) clearance on 1987-05-01, under 510(k) number K871480.

Who is the listed applicant for STD-228 SPECTRAL TREND DISPLAY?

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 STD-228 SPECTRAL TREND DISPLAY?

The FDA product code for STD-228 SPECTRAL TREND DISPLAY is GWS.

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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 OPTIONK974583DEEGLITEK974587H2OK972202DEEG-LITEK925838TELEFACTOR D/EEG-32K884937BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING

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Related Devices (Code: GWS)

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.

K974718PERSYST PRISMPersyst Development Corp.K925735EEG ANALYZERBio-Scan, Inc.K912938RHYTHMStellate SystemsK894629NICOLET BEAM II SYSTEMNicolet Instrument Corp.K871931ISTAT SOFTWARENeuroscience, Inc.K854662OEE_7102 EEG/TREND MONITORNihon Kohden America, 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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