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FDA 510(k)

DISPOSABLE NEEDLE ELECTRODE

K-Number: K961013 · 1996-12-20

Decision Date1996-12-20
Product CodeIKT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE NEEDLE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Medelec Intl. Corp.. It received FDA 510(k) clearance on 1996-12-20 under 510(k) number K961013. The device is classified under product code IKT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE NEEDLE ELECTRODE?

DISPOSABLE NEEDLE ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-12-20. The listed applicant is Medelec Intl. Corp.. The 510(k) number is K961013.

When did DISPOSABLE NEEDLE ELECTRODE receive FDA 510(k) clearance?

DISPOSABLE NEEDLE ELECTRODE received FDA 510(k) clearance on 1996-12-20, under 510(k) number K961013.

Who is the listed applicant for DISPOSABLE NEEDLE ELECTRODE?

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

What is the FDA product code for DISPOSABLE NEEDLE ELECTRODE?

The FDA product code for DISPOSABLE NEEDLE ELECTRODE is IKT.

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 Medelec Intl. Corp. 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 15 devices →

Related Devices (Code: IKT)

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

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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