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FDA 510(k)

DD-VCR-64

K-Number: K870381 · 1987-03-25

ApplicantGrass-Telefactor Product Group
Decision Date1987-03-25
Product CodeGWK
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DD-VCR-64 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 1987-03-25 under 510(k) number K870381. The device is classified under product code GWK. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DD-VCR-64?

DD-VCR-64 is a medical device that received FDA 510(k) clearance on 1987-03-25. The listed applicant is Grass-Telefactor Product Group. The 510(k) number is K870381.

When did DD-VCR-64 receive FDA 510(k) clearance?

DD-VCR-64 received FDA 510(k) clearance on 1987-03-25, under 510(k) number K870381.

Who is the listed applicant for DD-VCR-64?

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 DD-VCR-64?

The FDA product code for DD-VCR-64 is GWK.

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

View all 12 devices →

Related Devices (Code: GWK)

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.

K060919ACTICALRespironics, Inc.K061870VITALSENSE XHRRespironics, Inc.K052489ACTIHEARTRespironics, Inc.K991045MINI-LOGGER SERIES 2000Mini-Mitter Co., Inc.K905594NEUROFILE DATA STORAGE/ACCESORIES TO THE EEG-4300Nihon Kohden America, Inc.K904328VISTA POLYSOMNOGRAPHY COMPUTER SYSTEMTelediagnostic Systems, 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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