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FDA 510(k)

CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND

K-Number: K862734 · 1986-08-01

Decision Date1986-08-01
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND is the device name listed in this FDA 510(k) record. The listed applicant is D&R X-Ray Products, Inc.. It received FDA 510(k) clearance on 1986-08-01 under 510(k) number K862734. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND?

CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is D&R X-Ray Products, Inc.. The 510(k) number is K862734.

When did CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND receive FDA 510(k) clearance?

CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862734.

Who is the listed applicant for CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND?

The FDA 510(k) record lists D&R X-Ray Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND?

The FDA product code for CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND is IYB.

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 D&R X-Ray Products, Inc. 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: IYB)

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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