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FDA 510(k)

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV

K-Number: K820334 · 1982-03-15

ApplicantNemectron Medical, Inc.
Decision Date1982-03-15
Product Code
DecisionSubstantially Equivalent

Device Summary

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV 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 1982-03-15 under 510(k) number K820334. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV?

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is Nemectron Medical, Inc.. The 510(k) number is K820334.

When did NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV receive FDA 510(k) clearance?

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820334.

Who is the listed applicant for NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV?

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

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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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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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