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FDA 510(k)

ELECTROSTIMULI AVERSION MACHINE

K-Number: K820622 · 1982-04-09

ApplicantMichael R. Kiss
Decision Date1982-04-09
Product CodeHCB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROSTIMULI AVERSION MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Michael R. Kiss. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820622. The device is classified under product code HCB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSTIMULI AVERSION MACHINE?

ELECTROSTIMULI AVERSION MACHINE is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Michael R. Kiss. The 510(k) number is K820622.

When did ELECTROSTIMULI AVERSION MACHINE receive FDA 510(k) clearance?

ELECTROSTIMULI AVERSION MACHINE received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820622.

Who is the listed applicant for ELECTROSTIMULI AVERSION MACHINE?

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

What is the FDA product code for ELECTROSTIMULI AVERSION MACHINE?

The FDA product code for ELECTROSTIMULI AVERSION MACHINE is HCB.

Related Clinical Trials

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Related Devices (Code: HCB)

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.

K911820GED (GRADUATED ELECTRONIC DECELERATORBehavior Research Institute, Inc.K871158SIBIS REMOTE ACTUATORHuman Technologies, Inc.K853178SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEMOxford Medilog, Inc.K790738HABITSABATERJackson Ent.K760166STIMULATOR, SONIC CONTROL (AS-1)Farrall Instruments, Inc.

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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