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FDA 510(k)

FOCUS EMG

K-Number: K940050 · 1995-02-24

ApplicantFasstech
Decision Date1995-02-24
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FOCUS EMG is the device name listed in this FDA 510(k) record. The listed applicant is Fasstech. It received FDA 510(k) clearance on 1995-02-24 under 510(k) number K940050. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOCUS EMG?

FOCUS EMG is a medical device that received FDA 510(k) clearance on 1995-02-24. The listed applicant is Fasstech. The 510(k) number is K940050.

When did FOCUS EMG receive FDA 510(k) clearance?

FOCUS EMG received FDA 510(k) clearance on 1995-02-24, under 510(k) number K940050.

Who is the listed applicant for FOCUS EMG?

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

What is the FDA product code for FOCUS EMG?

The FDA product code for FOCUS EMG is HCC.

Related Clinical Trials

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Other records listing Fasstech 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.

K063447INSIGHT DISCOVERYK033452CWAS 1000K023209INSIGHT MILLENNIUM IIIK011964INSIGHT MILLENNIUM PLUSK011983INSIGHT GENESISK990778INSIGHT MILLENNIUM

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Related Devices (Code: HCC)

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.

K233580A Breathing System (ABS)Deepwell Dtx, Inc.K222101PrismGraymatters Health , Ltd.K180173FreespiraPalo Alto Health Sciences, Inc.K163448GrindCare SystemSunstar Suisse S.A.K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.K122879EEGER4 MODEL 4.3Eeg Software, 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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