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FDA 510(k)

ULTRASOUND TRANSMISSION GEL

K-Number: K842153 · 1984-07-18

ApplicantWpc Brands, Inc.
Decision Date1984-07-18
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRASOUND TRANSMISSION GEL is the device name listed in this FDA 510(k) record. The listed applicant is Wpc Brands, Inc.. It received FDA 510(k) clearance on 1984-07-18 under 510(k) number K842153. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASOUND TRANSMISSION GEL?

ULTRASOUND TRANSMISSION GEL is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Wpc Brands, Inc.. The 510(k) number is K842153.

When did ULTRASOUND TRANSMISSION GEL receive FDA 510(k) clearance?

ULTRASOUND TRANSMISSION GEL received FDA 510(k) clearance on 1984-07-18, under 510(k) number K842153.

Who is the listed applicant for ULTRASOUND TRANSMISSION GEL?

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

What is the FDA product code for ULTRASOUND TRANSMISSION GEL?

The FDA product code for ULTRASOUND TRANSMISSION GEL is IYO.

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.

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Other records listing Wpc Brands, 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.

K843167SONIC AID GREEN ULTRASOUND GEL

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.

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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