SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES
K-Number: K123980 · 2013-03-05
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Device Summary
Frequently Asked Questions
What is the SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES?
SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2013-03-05. The listed applicant is Misonix, Inc.. The 510(k) number is K123980.
When did SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES receive FDA 510(k) clearance?
SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES received FDA 510(k) clearance on 2013-03-05, under 510(k) number K123980.
Who is the listed applicant for SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES?
The FDA 510(k) record lists Misonix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES?
The FDA product code for SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES is NRB.
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 Misonix, 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: NRB)
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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