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FDA 510(k)

HAND-CARRIED ULTRASOUND SYSTEM

K-Number: K014116 · 2001-12-20

ApplicantSonosite,Inc.
Decision Date2001-12-20
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HAND-CARRIED ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sonosite,Inc.. It received FDA 510(k) clearance on 2001-12-20 under 510(k) number K014116. 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 HAND-CARRIED ULTRASOUND SYSTEM?

HAND-CARRIED ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2001-12-20. The listed applicant is Sonosite,Inc.. The 510(k) number is K014116.

When did HAND-CARRIED ULTRASOUND SYSTEM receive FDA 510(k) clearance?

HAND-CARRIED ULTRASOUND SYSTEM received FDA 510(k) clearance on 2001-12-20, under 510(k) number K014116.

Who is the listed applicant for HAND-CARRIED ULTRASOUND SYSTEM?

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

What is the FDA product code for HAND-CARRIED ULTRASOUND SYSTEM?

The FDA product code for HAND-CARRIED ULTRASOUND SYSTEM is IYN.

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Other records listing Sonosite,Inc. 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.

K113156SONOSITE EDGE ULTRASOUND SYSTEMK110645BIO Z CARDIO PROFILE HEMODYNAMIC MONITORK102390SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEMK093510LUMENVU CATHETER GUIDANCE SYSTEMK101757SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEMK092058SONOSITE NANOMAXX SERIES 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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