BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C
K-Number: K895034 · 1989-11-15
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Device Summary
Frequently Asked Questions
What is the BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C?
BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is Yamato Medical Corp.. The 510(k) number is K895034.
When did BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C receive FDA 510(k) clearance?
BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C received FDA 510(k) clearance on 1989-11-15, under 510(k) number K895034.
Who is the listed applicant for BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C?
The FDA 510(k) record lists Yamato Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C?
The FDA product code for BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C is IXY.
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: IXY)
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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