Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GED (GRADUATED ELECTRONIC DECELERATOR

K-Number: K911820 · 1994-12-05

ApplicantBehavior Research Institute, Inc.
Decision Date1994-12-05
Product CodeHCB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GED (GRADUATED ELECTRONIC DECELERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Behavior Research Institute, Inc.. It received FDA 510(k) clearance on 1994-12-05 under 510(k) number K911820. 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 GED (GRADUATED ELECTRONIC DECELERATOR?

GED (GRADUATED ELECTRONIC DECELERATOR is a medical device that received FDA 510(k) clearance on 1994-12-05. The listed applicant is Behavior Research Institute, Inc.. The 510(k) number is K911820.

When did GED (GRADUATED ELECTRONIC DECELERATOR receive FDA 510(k) clearance?

GED (GRADUATED ELECTRONIC DECELERATOR received FDA 510(k) clearance on 1994-12-05, under 510(k) number K911820.

Who is the listed applicant for GED (GRADUATED ELECTRONIC DECELERATOR?

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

What is the FDA product code for GED (GRADUATED ELECTRONIC DECELERATOR?

The FDA product code for GED (GRADUATED ELECTRONIC DECELERATOR is HCB.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K871158SIBIS REMOTE ACTUATORHuman Technologies, 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑