FDA 510(k)

IF-727 INTERFERENTIAL STIMULATOR

K-Number: K974585 · 1998-03-06

Decision Date1998-03-06

Product CodeLIH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

IF-727 INTERFERENTIAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Skylark Device Co., Ltd.. It received FDA 510(k) clearance on 1998-03-06 under 510(k) number K974585. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IF-727 INTERFERENTIAL STIMULATOR?

IF-727 INTERFERENTIAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1998-03-06. The listed applicant is Skylark Device Co., Ltd.. The 510(k) number is K974585.

When did IF-727 INTERFERENTIAL STIMULATOR receive FDA 510(k) clearance?

IF-727 INTERFERENTIAL STIMULATOR received FDA 510(k) clearance on 1998-03-06, under 510(k) number K974585.

Who is the listed applicant for IF-727 INTERFERENTIAL STIMULATOR?

The FDA 510(k) record lists Skylark Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IF-727 INTERFERENTIAL STIMULATOR?

The FDA product code for IF-727 INTERFERENTIAL STIMULATOR is LIH.

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 Skylark Device Co., Ltd. as applicant

K990233ST-302 INFRAREX K984506SD-100 SKYEAR THERMOMETER K981449SD-956 ULTRASOUND THERAPY K983964BATCH #6060 CONDUCTIVE GEL K964437GB-1002 TENS WITH MASSAGE K964434SD-970EMS ELECTRICAL MUSCULAR STIMULATOR

View all 20 devices →

Related Devices (Code: LIH)

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLC K183692Avid IF2Vision Quest Industries Inc./Dba VQ Orthocare K122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLC K110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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.