YOSHIDA AP 100
K-Number: K811211 · 1981-06-16
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Device Summary
Frequently Asked Questions
What is the YOSHIDA AP 100?
YOSHIDA AP 100 is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Kaycor Intl., Ltd.. The 510(k) number is K811211.
When did YOSHIDA AP 100 receive FDA 510(k) clearance?
YOSHIDA AP 100 received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811211.
Who is the listed applicant for YOSHIDA AP 100?
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 AP 100?
The FDA product code for YOSHIDA AP 100 is EGY.
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: EGY)
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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