RADIOGRAPHIC GRID
K-Number: K962338 · 1996-07-03
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Device Summary
Frequently Asked Questions
What is the RADIOGRAPHIC GRID?
RADIOGRAPHIC GRID is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Unidex Group, Inc.. The 510(k) number is K962338.
When did RADIOGRAPHIC GRID receive FDA 510(k) clearance?
RADIOGRAPHIC GRID received FDA 510(k) clearance on 1996-07-03, under 510(k) number K962338.
Who is the listed applicant for RADIOGRAPHIC GRID?
The FDA 510(k) record lists Unidex Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RADIOGRAPHIC GRID?
The FDA product code for RADIOGRAPHIC GRID is IXJ.
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 Unidex Group, 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: IXJ)
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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