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FDA 510(k)

YOSHIDA RIDO-F, MODEL LM-01

K-Number: K813348 · 1982-01-07

ApplicantKaycor Intl., Ltd.
Decision Date1982-01-07
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

YOSHIDA RIDO-F, MODEL LM-01 is the device name listed in this FDA 510(k) record. The listed applicant is Kaycor Intl., Ltd.. It received FDA 510(k) clearance on 1982-01-07 under 510(k) number K813348. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOSHIDA RIDO-F, MODEL LM-01?

YOSHIDA RIDO-F, MODEL LM-01 is a medical device that received FDA 510(k) clearance on 1982-01-07. The listed applicant is Kaycor Intl., Ltd.. The 510(k) number is K813348.

When did YOSHIDA RIDO-F, MODEL LM-01 receive FDA 510(k) clearance?

YOSHIDA RIDO-F, MODEL LM-01 received FDA 510(k) clearance on 1982-01-07, under 510(k) number K813348.

Who is the listed applicant for YOSHIDA RIDO-F, MODEL LM-01?

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

What is the FDA product code for YOSHIDA RIDO-F, MODEL LM-01?

The FDA product code for YOSHIDA RIDO-F, MODEL LM-01 is EKX.

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Other records listing Kaycor Intl., 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.

K965072PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNITK931717YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAYK832063ROBIN CORDLESS HANDPIECEK822740K30000 DENTAL CHAIRK811210YOSHIDA-PANOURA 10K811211YOSHIDA AP 100

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Related Devices (Code: EKX)

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.

K261987Reusable SmartPegOsstell ABK252223Alpha Endo Handpiece (Alpha Endo)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K251597InnerView SystemPerimetrics, Inc.K243692EnDrive (EnDriveUS)Advanced Technology Research (A.T.R.) S.R.L.K242514Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)Shenzhen Rogin Medical Co., Ltd.K241065ChecQ (AC100)Dentis Co., Ltd.

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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