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FDA 510(k)

BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C

K-Number: K895034 · 1989-11-15

Decision Date1989-11-15
Product CodeIXY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BUCKYS MODELS YMB-15A, YMB-15B AND YMB-15C is the device name listed in this FDA 510(k) record. The listed applicant is Yamato Medical Corp.. It received FDA 510(k) clearance on 1989-11-15 under 510(k) number K895034. The device is classified under product code IXY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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