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FDA 510(k)

US ALOKA SSD-256 ULTRASONIC SCANNER

K-Number: K813177 · 1982-03-05

ApplicantU. S. A. Imaging Corp.
Decision Date1982-03-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

US ALOKA SSD-256 ULTRASONIC SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is U. S. A. Imaging Corp.. It received FDA 510(k) clearance on 1982-03-05 under 510(k) number K813177. 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 US ALOKA SSD-256 ULTRASONIC SCANNER?

US ALOKA SSD-256 ULTRASONIC SCANNER is a medical device that received FDA 510(k) clearance on 1982-03-05. The listed applicant is U. S. A. Imaging Corp.. The 510(k) number is K813177.

When did US ALOKA SSD-256 ULTRASONIC SCANNER receive FDA 510(k) clearance?

US ALOKA SSD-256 ULTRASONIC SCANNER received FDA 510(k) clearance on 1982-03-05, under 510(k) number K813177.

Who is the listed applicant for US ALOKA SSD-256 ULTRASONIC SCANNER?

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

What is the FDA product code for US ALOKA SSD-256 ULTRASONIC SCANNER?

The FDA product code for US ALOKA SSD-256 ULTRASONIC SCANNER 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.

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Other records listing U. S. A. Imaging Corp. 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.

K813397SSD-240 ULTRASONIC SCANNERK813398SSD-203 ULTRASONIC SCANNER

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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