FDA 510(k)

STIMULATOR, SONIC CONTROL (AS-1)

K-Number: K760166 · 1976-07-20

Decision Date1976-07-20

Product CodeHCB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

STIMULATOR, SONIC CONTROL (AS-1) is the device name listed in this FDA 510(k) record. The listed applicant is Farrall Instruments, Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760166. 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 STIMULATOR, SONIC CONTROL (AS-1)?

STIMULATOR, SONIC CONTROL (AS-1) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Farrall Instruments, Inc.. The 510(k) number is K760166.

When did STIMULATOR, SONIC CONTROL (AS-1) receive FDA 510(k) clearance?

STIMULATOR, SONIC CONTROL (AS-1) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760166.

Who is the listed applicant for STIMULATOR, SONIC CONTROL (AS-1)?

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

What is the FDA product code for STIMULATOR, SONIC CONTROL (AS-1)?

The FDA product code for STIMULATOR, SONIC CONTROL (AS-1) 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Farrall Instruments, Inc. as applicant

K940128CAT-400UL PENILE PLETHYSMOGRAPH K936115CAT-600 PENILE PLETHYSMOGRAPH K821723BI-4520 DUAL IMPEDOMETER K821664PP-100, PERSONAL PERINEOMETER K792305A SLEEP ASSESSMENT DEVICE K781634VISUALAX

View all 7 devices →

Related Devices (Code: HCB)

K911820GED (GRADUATED ELECTRONIC DECELERATORBehavior Research Institute, Inc.K871158SIBIS REMOTE ACTUATORHuman Technologies, Inc.K853178SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEMOxford Medilog, Inc.K820622ELECTROSTIMULI AVERSION MACHINEMichael R. Kiss K790738HABITSABATERJackson Ent.

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.