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FDA 510(k)

SCANLUBE

K-Number: K031222 · 2003-07-23

ApplicantSonotech, Inc.
Decision Date2003-07-23
Product CodeMUI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCANLUBE is the device name listed in this FDA 510(k) record. The listed applicant is Sonotech, Inc.. It received FDA 510(k) clearance on 2003-07-23 under 510(k) number K031222. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANLUBE?

SCANLUBE is a medical device that received FDA 510(k) clearance on 2003-07-23. The listed applicant is Sonotech, Inc.. The 510(k) number is K031222.

When did SCANLUBE receive FDA 510(k) clearance?

SCANLUBE received FDA 510(k) clearance on 2003-07-23, under 510(k) number K031222.

Who is the listed applicant for SCANLUBE?

The FDA 510(k) record lists Sonotech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCANLUBE?

The FDA product code for SCANLUBE is MUI.

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Other records listing Sonotech, 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.

K042619ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANTK033178ULTRABIOK031894SCANTEC PADK013701ENDO-GLIDEK013170SCANTAC MEMBRANE OR SCANTAC STRIPK984562VIVOSONIC

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Related Devices (Code: MUI)

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.

K253255Non-Sterile Ultrasound Gel Sterile Ultrasound GelFoshan Pingchuang Medical Technology Co., Ltd.K252337EdgeFlow Gel PadEdgecare, Inc.K242167Sterile and Non-Sterile Ultrasonic Coupling AgentAnhui Deepblue Medical Technology Co., Ltd.K241789Non-Sterile Ultrasound Transmission GelsHony Medical Co., Ltd.K232957Sterile and Non-Sterile Ultrasound GelsJianerkang Medical Co., Ltd.K221999Ultrasound Transmission GelsHony Medical Co., Ltd.

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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