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FDA 510(k)

ELECTRODYN CII-INTERFERENTIAL MUSCLE

K-Number: K810513 · 1981-05-11

ApplicantNemectron Medical, Inc.
Decision Date1981-05-11
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRODYN CII-INTERFERENTIAL MUSCLE 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 1981-05-11 under 510(k) number K810513. 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 ELECTRODYN CII-INTERFERENTIAL MUSCLE?

ELECTRODYN CII-INTERFERENTIAL MUSCLE is a medical device that received FDA 510(k) clearance on 1981-05-11. The listed applicant is Nemectron Medical, Inc.. The 510(k) number is K810513.

When did ELECTRODYN CII-INTERFERENTIAL MUSCLE receive FDA 510(k) clearance?

ELECTRODYN CII-INTERFERENTIAL MUSCLE received FDA 510(k) clearance on 1981-05-11, under 510(k) number K810513.

Who is the listed applicant for ELECTRODYN CII-INTERFERENTIAL MUSCLE?

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 ELECTRODYN CII-INTERFERENTIAL MUSCLE?

The FDA product code for ELECTRODYN CII-INTERFERENTIAL MUSCLE is IPF.

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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 MICROWAVEK862376NEMECTROSON MODEL 2K854720NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.K854721NEMECTRODYN MODEL 2 & ENDOVAC 2K844416THERMOPULS E

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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.

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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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