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FDA 510(k)

BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING

K-Number: K884937 · 1989-04-14

ApplicantGrass-Telefactor Product Group
Decision Date1989-04-14
Product CodeEEG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING 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 1989-04-14 under 510(k) number K884937. The device is classified under product code EEG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING?

BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING is a medical device that received FDA 510(k) clearance on 1989-04-14. The listed applicant is Grass-Telefactor Product Group. The 510(k) number is K884937.

When did BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING receive FDA 510(k) clearance?

BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING received FDA 510(k) clearance on 1989-04-14, under 510(k) number K884937.

Who is the listed applicant for BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING?

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 BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING?

The FDA product code for BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING is EEG.

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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-32K870432A1-A2 AMBULATORY EEG CASSETTE RECORDER

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Related Devices (Code: EEG)

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.

K122725TANDA PEARL, ULTRAWYTE, PEARLSyneron BeautyK110888ABSOLUTE WHITE LIGHTDr. Fresh, Inc.K063704BRITEWHITE TEETH WHITENING SYSTEM, MODEL BW1101Beks IncorporatedK052040QUICKSMILECosmetic Dental Materials, Inc.K041392SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE USCAO Group, Inc.K042153SOUTH BEACH SMILE LIGHT WHITENING SYSTEMDentovations, 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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