STERILE EMG ELECTRODES
K-Number: K011818 · 2001-09-06
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Device Summary
Frequently Asked Questions
What is the STERILE EMG ELECTRODES?
STERILE EMG ELECTRODES is a medical device that received FDA 510(k) clearance on 2001-09-06. The listed applicant is Nicolet Biomedical, Inc.. The 510(k) number is K011818.
When did STERILE EMG ELECTRODES receive FDA 510(k) clearance?
STERILE EMG ELECTRODES received FDA 510(k) clearance on 2001-09-06, under 510(k) number K011818.
Who is the listed applicant for STERILE EMG ELECTRODES?
The FDA 510(k) record lists Nicolet Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE EMG ELECTRODES?
The FDA product code for STERILE EMG ELECTRODES 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 Nicolet Biomedical, 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.
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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