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FDA 510(k)

REX PEDESTAL INTRA-ORAL X-RAY UNIT

K-Number: K837491 · 1983-06-13

ApplicantThe Yoshida Dental Mfg. Co., Ltd.
Decision Date1983-06-13
Product Code
DecisionSubstantially Equivalent

Device Summary

REX PEDESTAL INTRA-ORAL 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 1983-06-13 under 510(k) number K837491. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REX PEDESTAL INTRA-ORAL X-RAY UNIT?

REX PEDESTAL INTRA-ORAL X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1983-06-13. The listed applicant is The Yoshida Dental Mfg. Co., Ltd.. The 510(k) number is K837491.

When did REX PEDESTAL INTRA-ORAL X-RAY UNIT receive FDA 510(k) clearance?

REX PEDESTAL INTRA-ORAL X-RAY UNIT received FDA 510(k) clearance on 1983-06-13, under 510(k) number K837491.

Who is the listed applicant for REX PEDESTAL INTRA-ORAL 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.

K182198Panoura X-ERA PF/NF/MFK122199PREXION3D ECLIPSEK120948PREXION 3DK120932OPELASER PRO II AND THE OPELASER LITE IIK111231PANOURA 18SK063622FINECUBE DENTAL CT

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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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