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FDA 510(k)

EPISON, ALERTING SYSTEM FOR EPILEPTICS

K-Number: K862766 · 1987-03-13

ApplicantZygo Industries, Inc.
Decision Date1987-03-13
Product CodeLEL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EPISON, ALERTING SYSTEM FOR EPILEPTICS is the device name listed in this FDA 510(k) record. The listed applicant is Zygo Industries, Inc.. It received FDA 510(k) clearance on 1987-03-13 under 510(k) number K862766. The device is classified under product code LEL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPISON, ALERTING SYSTEM FOR EPILEPTICS?

EPISON, ALERTING SYSTEM FOR EPILEPTICS is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is Zygo Industries, Inc.. The 510(k) number is K862766.

When did EPISON, ALERTING SYSTEM FOR EPILEPTICS receive FDA 510(k) clearance?

EPISON, ALERTING SYSTEM FOR EPILEPTICS received FDA 510(k) clearance on 1987-03-13, under 510(k) number K862766.

Who is the listed applicant for EPISON, ALERTING SYSTEM FOR EPILEPTICS?

The FDA 510(k) record lists Zygo Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPISON, ALERTING SYSTEM FOR EPILEPTICS?

The FDA product code for EPISON, ALERTING SYSTEM FOR EPILEPTICS is LEL.

Related Clinical Trials

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Other records listing Zygo Industries, Inc. 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.

K926029INFRA-LINKK924014SECRETARYK924013MACAWK924030SCRIBEK924015PARROT

Related Devices (Code: LEL)

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.

K252981EmbraceMiniEmpatica S.r.l.K251574Sleep WatchAmbulatory Monitoring, Inc.K243513DCM (PW-DCM)Pneumowave, Ltd.K233987VERABAND™Arbor Medical Innovations, LLCK233618Oxevision Sleep DeviceOxehealth LimitedK231532ActiGraph LEAP activity monitor (ActiGraph LEAP)Actigraph, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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