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FDA 510(k)

ELECTROSHOCK UNIT NEUROLOGY MODEL B-25

K-Number: K860467 · 1986-11-10

ApplicantMedcraft Corp.
Decision Date1986-11-10
Product CodeQGH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 is the device name listed in this FDA 510(k) record. The listed applicant is Medcraft Corp.. It received FDA 510(k) clearance on 1986-11-10 under 510(k) number K860467. 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 ELECTROSHOCK UNIT NEUROLOGY MODEL B-25?

ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 is a medical device that received FDA 510(k) clearance on 1986-11-10. The listed applicant is Medcraft Corp.. The 510(k) number is K860467.

When did ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 receive FDA 510(k) clearance?

ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 received FDA 510(k) clearance on 1986-11-10, under 510(k) number K860467.

Who is the listed applicant for ELECTROSHOCK UNIT NEUROLOGY MODEL B-25?

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

What is the FDA product code for ELECTROSHOCK UNIT NEUROLOGY MODEL B-25?

The FDA product code for ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 is QGH.

Related Clinical Trials

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Other records listing Medcraft Corp. 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.

K791795COMP-ACT IVK760510MONITORING SYSTEM, REHABILITATIONK760509TREADMILL, DIAGNOSTICK760508ACCUTAPE 24

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.K863815ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000Elcot, 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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