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FDA 510(k)

EXCEL EMG

K-Number: K941144 · 1995-11-07

ApplicantExcel Tech. , Ltd.
Decision Date1995-11-07
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EXCEL EMG is the device name listed in this FDA 510(k) record. The listed applicant is Excel Tech. , Ltd.. It received FDA 510(k) clearance on 1995-11-07 under 510(k) number K941144. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXCEL EMG?

EXCEL EMG is a medical device that received FDA 510(k) clearance on 1995-11-07. The listed applicant is Excel Tech. , Ltd.. The 510(k) number is K941144.

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

EXCEL EMG received FDA 510(k) clearance on 1995-11-07, under 510(k) number K941144.

Who is the listed applicant for EXCEL EMG?

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

What is the FDA product code for EXCEL EMG?

The FDA product code for EXCEL EMG is IKN.

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Other records listing Excel Tech. , Ltd. as applicant

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Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, Inc.

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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