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FDA 510(k)

NEMECTROSON MODEL 2

K-Number: K862376 · 1986-07-23

ApplicantNemectron Medical, Inc.
Decision Date1986-07-23
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEMECTROSON MODEL 2 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 1986-07-23 under 510(k) number K862376. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEMECTROSON MODEL 2?

NEMECTROSON MODEL 2 is a medical device that received FDA 510(k) clearance on 1986-07-23. The listed applicant is Nemectron Medical, Inc.. The 510(k) number is K862376.

When did NEMECTROSON MODEL 2 receive FDA 510(k) clearance?

NEMECTROSON MODEL 2 received FDA 510(k) clearance on 1986-07-23, under 510(k) number K862376.

Who is the listed applicant for NEMECTROSON MODEL 2?

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 NEMECTROSON MODEL 2?

The FDA product code for NEMECTROSON MODEL 2 is IMJ.

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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 MICROWAVEK854720NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.K854721NEMECTRODYN MODEL 2 & ENDOVAC 2K844416THERMOPULS EK843735SOFTEPIL

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Related Devices (Code: IMJ)

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.

K252963BTL-899TTBTL Industries, Inc.K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLC

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.

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