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FDA 510(k)

CYPRESS SYSTEM

K-Number: K010950 · 2001-06-27

ApplicantAcuson Corp.
Decision Date2001-06-27
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CYPRESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 2001-06-27 under 510(k) number K010950. 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 CYPRESS SYSTEM?

CYPRESS SYSTEM is a medical device that received FDA 510(k) clearance on 2001-06-27. The listed applicant is Acuson Corp.. The 510(k) number is K010950.

When did CYPRESS SYSTEM receive FDA 510(k) clearance?

CYPRESS SYSTEM received FDA 510(k) clearance on 2001-06-27, under 510(k) number K010950.

Who is the listed applicant for CYPRESS SYSTEM?

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

What is the FDA product code for CYPRESS SYSTEM?

The FDA product code for CYPRESS SYSTEM is IYO.

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Other records listing Acuson Corp. 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.

K023772KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEMK022896CSV12 SOFTWARE VIEWERK022567SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEMK021497CYPRESS ULTRASOUND SYSTEMK0028073D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSINGK992631ACUNAV DIAGNOSTIC ULTRASOUND CATHETER

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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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