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FDA 510(k)

ALOKA SSD-4000

K-Number: K003739 · 2000-12-27

ApplicantAloka Co., Ltd.
Decision Date2000-12-27
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALOKA SSD-4000 is the device name listed in this FDA 510(k) record. The listed applicant is Aloka Co., Ltd.. It received FDA 510(k) clearance on 2000-12-27 under 510(k) number K003739. 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 ALOKA SSD-4000?

ALOKA SSD-4000 is a medical device that received FDA 510(k) clearance on 2000-12-27. The listed applicant is Aloka Co., Ltd.. The 510(k) number is K003739.

When did ALOKA SSD-4000 receive FDA 510(k) clearance?

ALOKA SSD-4000 received FDA 510(k) clearance on 2000-12-27, under 510(k) number K003739.

Who is the listed applicant for ALOKA SSD-4000?

The FDA 510(k) record lists Aloka Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALOKA SSD-4000?

The FDA product code for ALOKA SSD-4000 is IYN.

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Other records listing Aloka Co., Ltd. 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.

K111227ALOKA SSD-3500 DIAGNOSTIC ULTRASOUND SYSTEMK110207ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEMK093488ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEMK083254ALOKA PROUSOUND 2 DIAGNOSTIC ULTRASOUND SYSTEMK081843ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1K080176ALOKA PROSOUND 6 DIAGNOSTIC ULTRASOUND SYSTEM

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Related Devices (Code: IYN)

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.

K262548EPIQ Inspira Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound SystemPhilips Ultrasound, LLCK263182EVO X30 Diagnostic Ultrasound System; EVO X20 Diagnostic Ultrasound System; EVO X10 Diagnostic Ultrasound System; EVO XP30 Diagnostic Ultrasound System; EVO XP20 Diagnostic Ultrasound System; EVO XP10 Diagnostic Ultrasound System; EVO XC30 Diagnostic Ultrasound System; EVO XC20 Diagnostic Ultrasound System; EVO XC10 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.K261313Vivid Explorer/Vivid Advanced/Vivid FocusGE Medical Systems Ultrasound and Primary Care DiagnosticsK254027Digital Color Doppler Ultrasound System (Marvo 95/Marvo 95 Elite/Marvo 90/Marvo 90 CV/Marvo 90 Pro/Marvo 90 Exp/Marvo 90 Elite/Marvo Expert/Marvo 85/Marvo 85 Pro/Marvo 85 Exp/Marvo 85 Elite/Marvo Senior/Marvo 75 Elite/Marvo 75i/Fenix 95/Fenix 95 Elite/Fenix 90/Fenix 90 Elite/Fenix Expert/Fenix 85/Fenix 85 Elite/Fenix Senior/Fenix 75 Elite/Fenix 75i/Endo 80/Endo 90)Sonoscape Medical Corp.K261668Venue GoGE Medical Systems Ultrasound and Primary care Diagnostics, LLCK262311Alturion Series Diagnostic Ultrasound SystemPhilips Ultrasound, LLC

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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