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FDA 510(k)

MODEL EM-2 BIOELECTRIC PROCESSOR

K-Number: K830034 · 1983-02-09

Decision Date1983-02-09
Product CodeKZM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL EM-2 BIOELECTRIC PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Myo-Tronics Research, Inc.. It received FDA 510(k) clearance on 1983-02-09 under 510(k) number K830034. The device is classified under product code KZM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL EM-2 BIOELECTRIC PROCESSOR?

MODEL EM-2 BIOELECTRIC PROCESSOR is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is Myo-Tronics Research, Inc.. The 510(k) number is K830034.

When did MODEL EM-2 BIOELECTRIC PROCESSOR receive FDA 510(k) clearance?

MODEL EM-2 BIOELECTRIC PROCESSOR received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830034.

Who is the listed applicant for MODEL EM-2 BIOELECTRIC PROCESSOR?

The FDA 510(k) record lists Myo-Tronics Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL EM-2 BIOELECTRIC PROCESSOR?

The FDA product code for MODEL EM-2 BIOELECTRIC PROCESSOR is KZM.

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.

Other records listing Myo-Tronics Research, 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.

View all 8 devices →

Related Devices (Code: KZM)

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.

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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