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FDA 510(k)

NEUROMUSCULAR ELECTRICAL STIMULATOR

K-Number: K940349 · 1994-04-01

ApplicantProgressive Concepts, Inc.
Decision Date1994-04-01
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEUROMUSCULAR ELECTRICAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Concepts, Inc.. It received FDA 510(k) clearance on 1994-04-01 under 510(k) number K940349. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMUSCULAR ELECTRICAL STIMULATOR?

NEUROMUSCULAR ELECTRICAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is Progressive Concepts, Inc.. The 510(k) number is K940349.

When did NEUROMUSCULAR ELECTRICAL STIMULATOR receive FDA 510(k) clearance?

NEUROMUSCULAR ELECTRICAL STIMULATOR received FDA 510(k) clearance on 1994-04-01, under 510(k) number K940349.

Who is the listed applicant for NEUROMUSCULAR ELECTRICAL STIMULATOR?

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

What is the FDA product code for NEUROMUSCULAR ELECTRICAL STIMULATOR?

The FDA product code for NEUROMUSCULAR ELECTRICAL STIMULATOR is IPF.

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 Progressive Concepts, Inc. 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.

K940600STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJK941959VERSATELL; VERSATELL-SK946298BIOSTIM-HV

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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