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)

NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.

K-Number: K854720 · 1986-03-10

ApplicantNemectron Medical, Inc.
Decision Date1986-03-10
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. is the device name listed in this FDA 510(k) record. The listed applicant is Nemectron Medical, Inc.. It received FDA 510(k) clearance on 1986-03-10 under 510(k) number K854720. 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 NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.?

NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. is a medical device that received FDA 510(k) clearance on 1986-03-10. The listed applicant is Nemectron Medical, Inc.. The 510(k) number is K854720.

When did NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. receive FDA 510(k) clearance?

NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. received FDA 510(k) clearance on 1986-03-10, under 510(k) number K854720.

Who is the listed applicant for NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.?

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

What is the FDA product code for NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.?

The FDA product code for NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. 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 Nemectron Medical, 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.

K923396THERMODYNK895000NEMECTRON MICROWAVEK862376NEMECTROSON MODEL 2K854721NEMECTRODYN MODEL 2 & ENDOVAC 2K844416THERMOPULS EK843735SOFTEPIL

View all 13 devices →

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

View on FDA Database →

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

↑