WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT
K-Number: K925934 · 1993-03-04
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Device Summary
Frequently Asked Questions
What is the WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT?
WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT is a medical device that received FDA 510(k) clearance on 1993-03-04. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K925934.
When did WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT receive FDA 510(k) clearance?
WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT received FDA 510(k) clearance on 1993-03-04, under 510(k) number K925934.
Who is the listed applicant for WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT?
The FDA 510(k) record lists Continental X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT?
The FDA product code for WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT 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.
Other records listing Continental X-Ray Corp. 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: 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
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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