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FDA 510(k)

YOSHIDA/KAYCOR X-70 X-RAY UNIT

K-Number: K828325 · 1982-10-21

ApplicantThe Yoshida Dental Mfg. Co., Ltd.
Decision Date1982-10-21
Product Code
DecisionSubstantially Equivalent

Device Summary

YOSHIDA/KAYCOR X-70 X-RAY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is The Yoshida Dental Mfg. Co., Ltd.. It received FDA 510(k) clearance on 1982-10-21 under 510(k) number K828325. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOSHIDA/KAYCOR X-70 X-RAY UNIT?

YOSHIDA/KAYCOR X-70 X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1982-10-21. The listed applicant is The Yoshida Dental Mfg. Co., Ltd.. The 510(k) number is K828325.

When did YOSHIDA/KAYCOR X-70 X-RAY UNIT receive FDA 510(k) clearance?

YOSHIDA/KAYCOR X-70 X-RAY UNIT received FDA 510(k) clearance on 1982-10-21, under 510(k) number K828325.

Who is the listed applicant for YOSHIDA/KAYCOR X-70 X-RAY UNIT?

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

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Other records listing The Yoshida Dental Mfg. 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

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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