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FDA 510(k)

DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20

K-Number: K896029 · 1990-01-12

ApplicantG.W.B. Intl., Ltd.
Decision Date1990-01-12
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20 is the device name listed in this FDA 510(k) record. The listed applicant is G.W.B. Intl., Ltd.. It received FDA 510(k) clearance on 1990-01-12 under 510(k) number K896029. 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 DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20?

DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20 is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is G.W.B. Intl., Ltd.. The 510(k) number is K896029.

When did DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20 receive FDA 510(k) clearance?

DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20 received FDA 510(k) clearance on 1990-01-12, under 510(k) number K896029.

Who is the listed applicant for DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20?

The FDA 510(k) record lists G.W.B. Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20?

The FDA product code for DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20 is IYO.

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Other records listing G.W.B. Intl., Ltd. as applicant

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Related Devices (Code: IYO)

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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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