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FDA 510(k)

DIAGNOSTIC ULTRASONIC TRANSDUCER

K-Number: K863364 · 1987-02-27

ApplicantToshiba Medical Systems
Decision Date1987-02-27
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC ULTRASONIC TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1987-02-27 under 510(k) number K863364. 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 DIAGNOSTIC ULTRASONIC TRANSDUCER?

DIAGNOSTIC ULTRASONIC TRANSDUCER is a medical device that received FDA 510(k) clearance on 1987-02-27. The listed applicant is Toshiba Medical Systems. The 510(k) number is K863364.

When did DIAGNOSTIC ULTRASONIC TRANSDUCER receive FDA 510(k) clearance?

DIAGNOSTIC ULTRASONIC TRANSDUCER received FDA 510(k) clearance on 1987-02-27, under 510(k) number K863364.

Who is the listed applicant for DIAGNOSTIC ULTRASONIC TRANSDUCER?

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

What is the FDA product code for DIAGNOSTIC ULTRASONIC TRANSDUCER?

The FDA product code for DIAGNOSTIC ULTRASONIC TRANSDUCER is ITX.

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Other records listing Toshiba Medical Systems 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.

K960948SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020AK954310BLA-800AK954309ANGIOREXK893750MRT-50A MOBILEK891453DIAGNOSTIC ULTRASOUND TRANSDUCER: PVE-582VK890969TRANSESOPHAGEAL TRANSDUCER PEF-511SA

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Related Devices (Code: ITX)

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.

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, 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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