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FDA 510(k)

YOSHIDA-PANOURA 10

K-Number: K811210 · 1981-08-24

ApplicantKaycor Intl., Ltd.
Decision Date1981-08-24
Product Code
DecisionSubstantially Equivalent

Device Summary

YOSHIDA-PANOURA 10 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 1981-08-24 under 510(k) number K811210. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOSHIDA-PANOURA 10?

YOSHIDA-PANOURA 10 is a medical device that received FDA 510(k) clearance on 1981-08-24. The listed applicant is Kaycor Intl., Ltd.. The 510(k) number is K811210.

When did YOSHIDA-PANOURA 10 receive FDA 510(k) clearance?

YOSHIDA-PANOURA 10 received FDA 510(k) clearance on 1981-08-24, under 510(k) number K811210.

Who is the listed applicant for YOSHIDA-PANOURA 10?

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

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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 CHAIRK813348YOSHIDA RIDO-F, MODEL LM-01K811211YOSHIDA AP 100

View all 7 devices →

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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