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FDA 510(k)

SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES

K-Number: K123980 · 2013-03-05

ApplicantMisonix, Inc.
Decision Date2013-03-05
Product CodeNRB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Misonix, Inc.. It received FDA 510(k) clearance on 2013-03-05 under 510(k) number K123980. The device is classified under product code NRB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 17 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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