YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY
K-Number: K931717 · 1993-09-20
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Device Summary
Frequently Asked Questions
What is the YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY?
YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Kaycor Intl., Ltd.. The 510(k) number is K931717.
When did YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY receive FDA 510(k) clearance?
YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY received FDA 510(k) clearance on 1993-09-20, under 510(k) number K931717.
Who is the listed applicant for YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY?
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/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY?
The FDA product code for YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY is EAP.
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 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.
Related Devices (Code: EAP)
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.
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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