NUFACE PLUS
K-Number: K103472 · 2011-11-07
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Device Summary
Frequently Asked Questions
What is the NUFACE PLUS?
NUFACE PLUS is a medical device that received FDA 510(k) clearance on 2011-11-07. The listed applicant is Carol Cole Company. The 510(k) number is K103472.
When did NUFACE PLUS receive FDA 510(k) clearance?
NUFACE PLUS received FDA 510(k) clearance on 2011-11-07, under 510(k) number K103472.
Who is the listed applicant for NUFACE PLUS?
The FDA 510(k) record lists Carol Cole Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NUFACE PLUS?
The FDA product code for NUFACE PLUS is NFO.
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 Carol Cole Company 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: NFO)
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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