FLUOROVIEW SERIES FLUOROSCOPIC TABLES
K-Number: K965096 · 1997-01-27
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Device Summary
Frequently Asked Questions
What is the FLUOROVIEW SERIES FLUOROSCOPIC TABLES?
FLUOROVIEW SERIES FLUOROSCOPIC TABLES is a medical device that received FDA 510(k) clearance on 1997-01-27. The listed applicant is U.S. Imaging Tables, Inc.. The 510(k) number is K965096.
When did FLUOROVIEW SERIES FLUOROSCOPIC TABLES receive FDA 510(k) clearance?
FLUOROVIEW SERIES FLUOROSCOPIC TABLES received FDA 510(k) clearance on 1997-01-27, under 510(k) number K965096.
Who is the listed applicant for FLUOROVIEW SERIES FLUOROSCOPIC TABLES?
The FDA 510(k) record lists U.S. Imaging Tables, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLUOROVIEW SERIES FLUOROSCOPIC TABLES?
The FDA product code for FLUOROVIEW SERIES FLUOROSCOPIC TABLES 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 U.S. Imaging Tables, 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: 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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