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FDA 510(k)

GL ULTRASOUND Z/SL 8300

K-Number: K843205 · 1985-02-25

ApplicantGl Ultrasound , Ltd.
Decision Date1985-02-25
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GL ULTRASOUND Z/SL 8300 is the device name listed in this FDA 510(k) record. The listed applicant is Gl Ultrasound , Ltd.. It received FDA 510(k) clearance on 1985-02-25 under 510(k) number K843205. 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 GL ULTRASOUND Z/SL 8300?

GL ULTRASOUND Z/SL 8300 is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Gl Ultrasound , Ltd.. The 510(k) number is K843205.

When did GL ULTRASOUND Z/SL 8300 receive FDA 510(k) clearance?

GL ULTRASOUND Z/SL 8300 received FDA 510(k) clearance on 1985-02-25, under 510(k) number K843205.

Who is the listed applicant for GL ULTRASOUND Z/SL 8300?

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

What is the FDA product code for GL ULTRASOUND Z/SL 8300?

The FDA product code for GL ULTRASOUND Z/SL 8300 is IYO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Gl Ultrasound , 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.

K854555GL590 DIAGNOSTIC ULTRASOUND EQUIPMENTK844393GL ULTRASOUND SECTOR 170

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.

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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