DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004
K-Number: K921501 · 1992-05-15
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Device Summary
Frequently Asked Questions
What is the DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004?
DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004 is a medical device that received FDA 510(k) clearance on 1992-05-15. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K921501.
When did DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004 receive FDA 510(k) clearance?
DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004 received FDA 510(k) clearance on 1992-05-15, under 510(k) number K921501.
Who is the listed applicant for DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004?
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 DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004?
The FDA product code for DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004 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 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: 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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