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FDA 510(k)

ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K920374 · 1992-04-02

ApplicantGe Medical Systems Information Technologies
Decision Date1992-04-02
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1992-04-02 under 510(k) number K920374. 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 ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM?

ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1992-04-02. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K920374.

When did ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 1992-04-02, under 510(k) number K920374.

Who is the listed applicant for ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM is 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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