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FDA 510(k)

CERSR ELECTROMYOGRAPHY SYSTEM

K-Number: K990766 · 1999-08-27

ApplicantParaspinal Diagnostic Corp.
Decision Date1999-08-27
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CERSR ELECTROMYOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Paraspinal Diagnostic Corp.. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K990766. 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 CERSR ELECTROMYOGRAPHY SYSTEM?

CERSR ELECTROMYOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Paraspinal Diagnostic Corp.. The 510(k) number is K990766.

When did CERSR ELECTROMYOGRAPHY SYSTEM receive FDA 510(k) clearance?

CERSR ELECTROMYOGRAPHY SYSTEM received FDA 510(k) clearance on 1999-08-27, under 510(k) number K990766.

Who is the listed applicant for CERSR ELECTROMYOGRAPHY SYSTEM?

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

What is the FDA product code for CERSR ELECTROMYOGRAPHY SYSTEM?

The FDA product code for CERSR ELECTROMYOGRAPHY SYSTEM is IKN.

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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

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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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