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FDA 510(k)

BUCKY WALL STAND

K-Number: K781473 · 1978-09-11

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1978-09-11
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BUCKY WALL STAND is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1978-09-11 under 510(k) number K781473. 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 BUCKY WALL STAND?

BUCKY WALL STAND is a medical device that received FDA 510(k) clearance on 1978-09-11. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K781473.

When did BUCKY WALL STAND receive FDA 510(k) clearance?

BUCKY WALL STAND received FDA 510(k) clearance on 1978-09-11, under 510(k) number K781473.

Who is the listed applicant for BUCKY WALL STAND?

The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUCKY WALL STAND?

The FDA product code for BUCKY WALL STAND 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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