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FDA 510(k)

ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000

K-Number: K863815 · 1987-06-02

ApplicantElcot, Inc.
Decision Date1987-06-02
Product CodeQGH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Elcot, Inc.. It received FDA 510(k) clearance on 1987-06-02 under 510(k) number K863815. The device is classified under product code QGH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000?

ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 is a medical device that received FDA 510(k) clearance on 1987-06-02. The listed applicant is Elcot, Inc.. The 510(k) number is K863815.

When did ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 receive FDA 510(k) clearance?

ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 received FDA 510(k) clearance on 1987-06-02, under 510(k) number K863815.

Who is the listed applicant for ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000?

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

What is the FDA product code for ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000?

The FDA product code for ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 is QGH.

Related Clinical Trials

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.

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Other records listing Elcot, 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.

K911144MF-500, MODIFICATION

Related Devices (Code: QGH)

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.

K192834MECTA SigmaMecta CorporationK965070SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.Mecta Corp.K960754SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 MMecta Corp.K945120THYMATRON 2000 ELECTROCONVULSIVE SYSTEMSomatics, Inc.K911144MF-500, MODIFICATIONElcot, Inc.K860467ELECTROSHOCK UNIT NEUROLOGY MODEL B-25Medcraft Corp.

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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