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FDA 510(k)

MECTA ECT DEVICE MODELS SR & JR

K-Number: K852069 · 1985-08-09

ApplicantMecta Corp.
Decision Date1985-08-09
Product CodeQGH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MECTA ECT DEVICE MODELS SR & JR is the device name listed in this FDA 510(k) record. The listed applicant is Mecta Corp.. It received FDA 510(k) clearance on 1985-08-09 under 510(k) number K852069. 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 MECTA ECT DEVICE MODELS SR & JR?

MECTA ECT DEVICE MODELS SR & JR is a medical device that received FDA 510(k) clearance on 1985-08-09. The listed applicant is Mecta Corp.. The 510(k) number is K852069.

When did MECTA ECT DEVICE MODELS SR & JR receive FDA 510(k) clearance?

MECTA ECT DEVICE MODELS SR & JR received FDA 510(k) clearance on 1985-08-09, under 510(k) number K852069.

Who is the listed applicant for MECTA ECT DEVICE MODELS SR & JR?

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

What is the FDA product code for MECTA ECT DEVICE MODELS SR & JR?

The FDA product code for MECTA ECT DEVICE MODELS SR & JR 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 Mecta 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.

K965070SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.K960754SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M

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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