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FDA 510(k)

HABITSABATER

K-Number: K790738 · 1979-06-20

ApplicantJackson Ent.
Decision Date1979-06-20
Product CodeHCB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HABITSABATER is the device name listed in this FDA 510(k) record. The listed applicant is Jackson Ent.. It received FDA 510(k) clearance on 1979-06-20 under 510(k) number K790738. 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 HABITSABATER?

HABITSABATER is a medical device that received FDA 510(k) clearance on 1979-06-20. The listed applicant is Jackson Ent.. The 510(k) number is K790738.

When did HABITSABATER receive FDA 510(k) clearance?

HABITSABATER received FDA 510(k) clearance on 1979-06-20, under 510(k) number K790738.

Who is the listed applicant for HABITSABATER?

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

What is the FDA product code for HABITSABATER?

The FDA product code for HABITSABATER is HCB.

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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.K820622ELECTROSTIMULI AVERSION MACHINEMichael R. KissK760166STIMULATOR, SONIC CONTROL (AS-1)Farrall Instruments, 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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