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FDA 510(k)

BUCKYMAT

K-Number: K790069 · 1979-01-26

ApplicantSiemens Corp.
Decision Date1979-01-26
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BUCKYMAT is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K790069. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUCKYMAT?

BUCKYMAT is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Siemens Corp.. The 510(k) number is K790069.

When did BUCKYMAT receive FDA 510(k) clearance?

BUCKYMAT received FDA 510(k) clearance on 1979-01-26, under 510(k) number K790069.

Who is the listed applicant for BUCKYMAT?

The FDA 510(k) record lists Siemens Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUCKYMAT?

The FDA product code for BUCKYMAT is KPR.

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Related Devices (Code: KPR)

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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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