UROLOGICAL C-ARM TABLE, MODEL #056-450
K-Number: K922591 · 1992-11-27
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Device Summary
Frequently Asked Questions
What is the UROLOGICAL C-ARM TABLE, MODEL #056-450?
UROLOGICAL C-ARM TABLE, MODEL #056-450 is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K922591.
When did UROLOGICAL C-ARM TABLE, MODEL #056-450 receive FDA 510(k) clearance?
UROLOGICAL C-ARM TABLE, MODEL #056-450 received FDA 510(k) clearance on 1992-11-27, under 510(k) number K922591.
Who is the listed applicant for UROLOGICAL C-ARM TABLE, MODEL #056-450?
The FDA 510(k) record lists Biodan Medical Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UROLOGICAL C-ARM TABLE, MODEL #056-450?
The FDA product code for UROLOGICAL C-ARM TABLE, MODEL #056-450 is IXR.
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 Biodan Medical Systems, Ltd. 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: IXR)
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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