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FDA 510(k)

SIBIS REMOTE ACTUATOR

K-Number: K871158 · 1987-05-29

ApplicantHuman Technologies, Inc.
Decision Date1987-05-29
Product CodeHCB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SIBIS REMOTE ACTUATOR is the device name listed in this FDA 510(k) record. The listed applicant is Human Technologies, Inc.. It received FDA 510(k) clearance on 1987-05-29 under 510(k) number K871158. 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 SIBIS REMOTE ACTUATOR?

SIBIS REMOTE ACTUATOR is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is Human Technologies, Inc.. The 510(k) number is K871158.

When did SIBIS REMOTE ACTUATOR receive FDA 510(k) clearance?

SIBIS REMOTE ACTUATOR received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871158.

Who is the listed applicant for SIBIS REMOTE ACTUATOR?

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

What is the FDA product code for SIBIS REMOTE ACTUATOR?

The FDA product code for SIBIS REMOTE ACTUATOR is HCB.

Related Clinical Trials

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Other records listing Human Technologies, 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.

K880639ACCUTEMP(TM) TEMP. MONITIORING SYSTEM SWALLOWABLEK871203BED PATIENT PRESENCE MONITOR

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.K853178SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEMOxford Medilog, Inc.K820622ELECTROSTIMULI AVERSION MACHINEMichael R. KissK790738HABITSABATERJackson 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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