YOBOSHI DENTAL UNIT
K-Number: K103550 · 2011-01-04
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Device Summary
Frequently Asked Questions
What is the YOBOSHI DENTAL UNIT?
YOBOSHI DENTAL UNIT is a medical device that received FDA 510(k) clearance on 2011-01-04. The listed applicant is Fosham Yoboshi Medical Equipment Co., Ltd.. The 510(k) number is K103550.
When did YOBOSHI DENTAL UNIT receive FDA 510(k) clearance?
YOBOSHI DENTAL UNIT received FDA 510(k) clearance on 2011-01-04, under 510(k) number K103550.
Who is the listed applicant for YOBOSHI DENTAL UNIT?
The FDA 510(k) record lists Fosham Yoboshi Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YOBOSHI DENTAL UNIT?
The FDA product code for YOBOSHI DENTAL UNIT is EIA.
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.
Related Devices (Code: EIA)
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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