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FDA 510(k)

ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM

K-Number: K905252 · 1991-02-12

ApplicantGe Medical Systems Information Technologies
Decision Date1991-02-12
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING 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 1991-02-12 under 510(k) number K905252. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM?

ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM is a medical device that received FDA 510(k) clearance on 1991-02-12. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K905252.

When did ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM receive FDA 510(k) clearance?

ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM received FDA 510(k) clearance on 1991-02-12, under 510(k) number K905252.

Who is the listed applicant for ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING 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 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM?

The FDA product code for ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM is ITX.

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Other records listing Ge Medical Systems Information Technologies as applicant

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Related Devices (Code: ITX)

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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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