CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND
K-Number: K862734 · 1986-08-01
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Device Summary
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
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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