Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE

K-Number: K955335 · 1996-01-29

Decision Date1996-01-29
Product CodeIKT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Chalgren Enterprises, Inc.. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K955335. 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 HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE?

DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is Chalgren Enterprises, Inc.. The 510(k) number is K955335.

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

DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE received FDA 510(k) clearance on 1996-01-29, under 510(k) number K955335.

Who is the listed applicant for DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE?

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

What is the FDA product code for DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE?

The FDA product code for DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING 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 Chalgren Enterprises, 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 21 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.

↑