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FDA 510(k)

LTRASONIC SCANNER U.S. ALOKA SSD-500

K-Number: K827177 · 1982-04-25

Decision Date1982-04-25
Product Code
DecisionSubstantially Equivalent

Device Summary

LTRASONIC SCANNER U.S. ALOKA SSD-500 is the device name listed in this FDA 510(k) record. The listed applicant is Aloka Co., Ltd.. It received FDA 510(k) clearance on 1982-04-25 under 510(k) number K827177. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LTRASONIC SCANNER U.S. ALOKA SSD-500?

LTRASONIC SCANNER U.S. ALOKA SSD-500 is a medical device that received FDA 510(k) clearance on 1982-04-25. The listed applicant is Aloka Co., Ltd.. The 510(k) number is K827177.

When did LTRASONIC SCANNER U.S. ALOKA SSD-500 receive FDA 510(k) clearance?

LTRASONIC SCANNER U.S. ALOKA SSD-500 received FDA 510(k) clearance on 1982-04-25, under 510(k) number K827177.

Who is the listed applicant for LTRASONIC SCANNER U.S. ALOKA SSD-500?

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

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.

Other records listing Aloka Co., 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.

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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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