BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY
K-Number: K924445 · 1993-02-19
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Device Summary
Frequently Asked Questions
What is the BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY?
BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY is a medical device that received FDA 510(k) clearance on 1993-02-19. The listed applicant is Control-X, Inc.. The 510(k) number is K924445.
When did BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY receive FDA 510(k) clearance?
BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY received FDA 510(k) clearance on 1993-02-19, under 510(k) number K924445.
Who is the listed applicant for BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY?
The FDA 510(k) record lists Control-X, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY?
The FDA product code for BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY 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 Control-X, 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: 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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