FDA 510(k)

DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER

K-Number: K951998 · 1996-03-27

Decision Date1996-03-27

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics Ultrasound. It received FDA 510(k) clearance on 1996-03-27 under 510(k) number K951998. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER?

DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is Diasonics Ultrasound. The 510(k) number is K951998.

When did DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER receive FDA 510(k) clearance?

DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER received FDA 510(k) clearance on 1996-03-27, under 510(k) number K951998.

Who is the listed applicant for DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER?

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

What is the FDA product code for DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER?

The FDA product code for DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER is IYN.

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Other records listing Diasonics Ultrasound as applicant

K961002DIASONICS ITNRAOPERATIVE PROBES

Related Devices (Code: IYN)

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.