ULTRASONIC SCALER
K-Number: K113530 · 2013-01-31
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Device Summary
Frequently Asked Questions
What is the ULTRASONIC SCALER?
ULTRASONIC SCALER is a medical device that received FDA 510(k) clearance on 2013-01-31. The listed applicant is Nakanishi, Inc.. The 510(k) number is K113530.
When did ULTRASONIC SCALER receive FDA 510(k) clearance?
ULTRASONIC SCALER received FDA 510(k) clearance on 2013-01-31, under 510(k) number K113530.
Who is the listed applicant for ULTRASONIC SCALER?
The FDA 510(k) record lists Nakanishi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRASONIC SCALER?
The FDA product code for ULTRASONIC SCALER is ELC.
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 Nakanishi, 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: ELC)
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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