SOYEE ALUMINUM INTERSPACED X-RAY GRID
K-Number: K926445 · 1993-04-07
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Device Summary
Frequently Asked Questions
What is the SOYEE ALUMINUM INTERSPACED X-RAY GRID?
SOYEE ALUMINUM INTERSPACED X-RAY GRID is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is X-Ray Accessories Mfg. Co.. The 510(k) number is K926445.
When did SOYEE ALUMINUM INTERSPACED X-RAY GRID receive FDA 510(k) clearance?
SOYEE ALUMINUM INTERSPACED X-RAY GRID received FDA 510(k) clearance on 1993-04-07, under 510(k) number K926445.
Who is the listed applicant for SOYEE ALUMINUM INTERSPACED X-RAY GRID?
The FDA 510(k) record lists X-Ray Accessories Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOYEE ALUMINUM INTERSPACED X-RAY GRID?
The FDA product code for SOYEE ALUMINUM INTERSPACED X-RAY 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 X-Ray Accessories Mfg. Co. 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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