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FDA 510(k)

PC 2909A-HEALTH PULSE CONTROL STIMULATOR

K-Number: K830747 · 1983-05-30

ApplicantJ.A. Preston Corp.
Decision Date1983-05-30
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PC 2909A-HEALTH PULSE CONTROL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is J.A. Preston Corp.. It received FDA 510(k) clearance on 1983-05-30 under 510(k) number K830747. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PC 2909A-HEALTH PULSE CONTROL STIMULATOR?

PC 2909A-HEALTH PULSE CONTROL STIMULATOR is a medical device that received FDA 510(k) clearance on 1983-05-30. The listed applicant is J.A. Preston Corp.. The 510(k) number is K830747.

When did PC 2909A-HEALTH PULSE CONTROL STIMULATOR receive FDA 510(k) clearance?

PC 2909A-HEALTH PULSE CONTROL STIMULATOR received FDA 510(k) clearance on 1983-05-30, under 510(k) number K830747.

Who is the listed applicant for PC 2909A-HEALTH PULSE CONTROL STIMULATOR?

The FDA 510(k) record lists J.A. Preston Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PC 2909A-HEALTH PULSE CONTROL STIMULATOR?

The FDA product code for PC 2909A-HEALTH PULSE CONTROL STIMULATOR is GZJ.

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

Other records listing J.A. Preston Corp. 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.

K861739TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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