B-4 FOUR-WAY RADIOGRAPHIC TABLE
K-Number: K924444 · 1993-02-05
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Device Summary
Frequently Asked Questions
What is the B-4 FOUR-WAY RADIOGRAPHIC TABLE?
B-4 FOUR-WAY RADIOGRAPHIC TABLE is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Control-X, Inc.. The 510(k) number is K924444.
When did B-4 FOUR-WAY RADIOGRAPHIC TABLE receive FDA 510(k) clearance?
B-4 FOUR-WAY RADIOGRAPHIC TABLE received FDA 510(k) clearance on 1993-02-05, under 510(k) number K924444.
Who is the listed applicant for B-4 FOUR-WAY RADIOGRAPHIC TABLE?
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 B-4 FOUR-WAY RADIOGRAPHIC TABLE?
The FDA product code for B-4 FOUR-WAY RADIOGRAPHIC TABLE is IZZ.
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: IZZ)
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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