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FDA 510(k)

VISION DIAGNOSTIC ULTRASONIC SCANNER

K-Number: K901467 · 1990-09-05

ApplicantThe Probe Corp.
Decision Date1990-09-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISION DIAGNOSTIC ULTRASONIC SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is The Probe Corp.. It received FDA 510(k) clearance on 1990-09-05 under 510(k) number K901467. 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 VISION DIAGNOSTIC ULTRASONIC SCANNER?

VISION DIAGNOSTIC ULTRASONIC SCANNER is a medical device that received FDA 510(k) clearance on 1990-09-05. The listed applicant is The Probe Corp.. The 510(k) number is K901467.

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

VISION DIAGNOSTIC ULTRASONIC SCANNER received FDA 510(k) clearance on 1990-09-05, under 510(k) number K901467.

Who is the listed applicant for VISION DIAGNOSTIC ULTRASONIC SCANNER?

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

What is the FDA product code for VISION DIAGNOSTIC ULTRASONIC SCANNER?

The FDA product code for VISION DIAGNOSTIC ULTRASONIC SCANNER is IYO.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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